Diltiazem Hydrochloride (Page 6 of 6)

PRINCIPAL DISPLAY PANEL

NDC 62037-691-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
180 mg
Watson 30 Tablets Rx only

NDC 62037-691-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
180 mg 
Watson   30 Tablets     Rx only
(click image for full-size original)

NDC 62037-691-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
180 mg Watson 90 Tablets Rx only

NDC 62037-691-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
180 mg 
Watson   90 Tablets     Rx only
(click image for full-size original)

NDC 62037-692-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
240 mg
Watson 30 Tablets Rx only

NDC 62037-692-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
240 mg 
Watson  30 Tablets     Rx only
(click image for full-size original)

NDC 62037-693-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
300 mg Watson 30 Tablets Rx only

NDC 62037-693-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
300 mg 
Watson   30 Tablets     Rx only
(click image for full-size original)

NDC 62037-693-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
300 mg Watson 90 Tablets Rx only

NDC 62037-693-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
300 mg 
Watson   90 Tablets     Rx only
(click image for full-size original)

NDC 62037-694-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
360 mg Watson 30 Tablets Rx only

NDC 62037-694-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
360 mg 
Watson   30 Tablets     Rx only
(click image for full-size original)

NDC 62037-694-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
360 mg Watson 90 Tablets Rx only

NDC 62037-694-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
360 mg 
Watson   90 Tablets     Rx only
(click image for full-size original)

NDC 62037-695-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
420 mg Watson 30 Tablets Rx only

NDC 62037-695-30
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
420 mg 
Watson   30 Tablets     Rx only
(click image for full-size original)

NDC 62037-695-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
420 mg Watson 90 Tablets Rx only

NDC 62037-695-90
Matzim™ LA
(Diltiazem Hydrochloride)
Extended-release Tablets
Once-a-day Dosage
420 mg 
Watson   90 Tablets     Rx only
(click image for full-size original)
DILTIAZEM HYDROCHLORIDE diltiazem hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62037-690
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DILTIAZEM HYDROCHLORIDE (DILTIAZEM) DILTIAZEM HYDROCHLORIDE 120 mg
Inactive Ingredients
Ingredient Name Strength
CANDELILLA WAX
SILICON DIOXIDE
STARCH, CORN
ETHYLCELLULOSES
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
NONOXYNOL-100
POLYETHYLENE GLYCOL
POLYSORBATE 80
POVIDONE K30
SUCROSE
TALC
TITANIUM DIOXIDE
TRIACETIN
HYPROMELLOSE 2910 (15 MPA.S)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW)
Product Characteristics
Color WHITE (WHITE) Score no score
Shape CAPSULE (CAPSULE) Size 13mm
Flavor Imprint Code 120;690
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62037-690-10 1000 TABLET, EXTENDED RELEASE (1000 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:62037-690-30 30 TABLET, EXTENDED RELEASE (30 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:62037-690-90 90 TABLET, EXTENDED RELEASE (90 TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077686 03/15/2010
DILTIAZEM HYDROCHLORIDE diltiazem hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62037-691
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DILTIAZEM HYDROCHLORIDE (DILTIAZEM) DILTIAZEM HYDROCHLORIDE 180 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
STARCH, CORN
ETHYLCELLULOSES
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
NONOXYNOL-100
POLYETHYLENE GLYCOL
POLYSORBATE 80
POVIDONE K30
SUCROSE
TALC
TITANIUM DIOXIDE
TRIACETIN
CANDELILLA WAX
HYPROMELLOSE 2910 (15 MPA.S)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW)
Product Characteristics
Color WHITE (WHITE) Score no score
Shape CAPSULE (CAPSULE) Size 15mm
Flavor Imprint Code 180;691
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62037-691-10 1000 TABLET, EXTENDED RELEASE (1000 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:62037-691-30 30 TABLET, EXTENDED RELEASE (30 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:62037-691-90 90 TABLET, EXTENDED RELEASE (90 TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077686 03/15/2010
DILTIAZEM HYDROCHLORIDE diltiazem hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62037-692
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DILTIAZEM HYDROCHLORIDE (DILTIAZEM) DILTIAZEM HYDROCHLORIDE 240 mg
Inactive Ingredients
Ingredient Name Strength
CANDELILLA WAX
SILICON DIOXIDE
STARCH, CORN
ETHYLCELLULOSES
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
NONOXYNOL-100
POLYETHYLENE GLYCOL
POLYSORBATE 80
POVIDONE K30
SUCROSE
TALC
TITANIUM DIOXIDE
TRIACETIN
HYPROMELLOSE 2910 (15 MPA.S)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW)
Product Characteristics
Color WHITE (WHITE) Score no score
Shape CAPSULE (CAPSULE) Size 16mm
Flavor Imprint Code 240;692
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62037-692-10 1000 TABLET, EXTENDED RELEASE (1000 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:62037-692-30 30 TABLET, EXTENDED RELEASE (30 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:62037-692-90 90 TABLET, EXTENDED RELEASE (90 TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077686 03/15/2010
DILTIAZEM HYDROCHLORIDE diltiazem hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62037-693
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DILTIAZEM HYDROCHLORIDE (DILTIAZEM) DILTIAZEM HYDROCHLORIDE 300 mg
Inactive Ingredients
Ingredient Name Strength
CANDELILLA WAX
SILICON DIOXIDE
STARCH, CORN
ETHYLCELLULOSES
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
NONOXYNOL-100
POLYETHYLENE GLYCOL
POLYSORBATE 80
POVIDONE K30
SUCROSE
TALC
TITANIUM DIOXIDE
TRIACETIN
HYPROMELLOSE 2910 (15 MPA.S)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW)
Product Characteristics
Color WHITE (WHITE) Score no score
Shape CAPSULE (CAPSULE) Size 18mm
Flavor Imprint Code 300;693
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62037-693-10 1000 TABLET, EXTENDED RELEASE (1000 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:62037-693-30 30 TABLET, EXTENDED RELEASE (30 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:62037-693-90 90 TABLET, EXTENDED RELEASE (90 TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077686 03/15/2010
DILTIAZEM HYDROCHLORIDE diltiazem hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62037-694
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DILTIAZEM HYDROCHLORIDE (DILTIAZEM) DILTIAZEM HYDROCHLORIDE 360 mg
Inactive Ingredients
Ingredient Name Strength
CANDELILLA WAX
SILICON DIOXIDE
STARCH, CORN
ETHYLCELLULOSES
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
NONOXYNOL-100
POLYETHYLENE GLYCOL
POLYSORBATE 80
POVIDONE K30
SUCROSE
TALC
TITANIUM DIOXIDE
TRIACETIN
HYPROMELLOSE 2910 (15 MPA.S)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW)
Product Characteristics
Color WHITE (WHITE) Score no score
Shape CAPSULE (CAPSULE) Size 19mm
Flavor Imprint Code 360;694
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62037-694-10 1000 TABLET, EXTENDED RELEASE (1000 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:62037-694-30 30 TABLET, EXTENDED RELEASE (30 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:62037-694-90 90 TABLET, EXTENDED RELEASE (90 TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077686 03/15/2010
DILTIAZEM HYDROCHLORIDE diltiazem hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62037-695
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DILTIAZEM HYDROCHLORIDE (DILTIAZEM) DILTIAZEM HYDROCHLORIDE 420 mg
Inactive Ingredients
Ingredient Name Strength
CANDELILLA WAX
SILICON DIOXIDE
STARCH, CORN
ETHYLCELLULOSES
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
NONOXYNOL-100
POLYETHYLENE GLYCOL
POLYSORBATE 80
POVIDONE K30
SUCROSE
TALC
TITANIUM DIOXIDE
TRIACETIN
HYPROMELLOSE 2910 (15 MPA.S)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 600000 MW)
Product Characteristics
Color WHITE (WHITE) Score no score
Shape CAPSULE (CAPSULE) Size 19mm
Flavor Imprint Code 420;695
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62037-695-10 1000 TABLET, EXTENDED RELEASE (1000 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:62037-695-30 30 TABLET, EXTENDED RELEASE (30 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:62037-695-90 90 TABLET, EXTENDED RELEASE (90 TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077686 03/15/2010
Labeler — Watson Pharma, Inc. (966714656)
Establishment
Name Address ID/FEI Operations
Watson Laboratories, Inc. — Florida 020778751 MANUFACTURE

Revised: 05/2011 Watson Pharma, Inc.

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