Fosinopril Sodium (Page 7 of 7)

Package/Label Display Panel – 20 mg

Container Label — 20 mg — 90 tablets

NDC 43547-387-09 Rx only

Fosinopril Sodium Tablets,USP

20 mg

90 Tablets

Each tablet contains:

20 mg of Fosinopril Sodium, USP.

Usual dosage: See package insert for full prescribing information.

Store at 20°C to 25°C (68°F to 77°F)

[See USP Controlled Room Temperature]

Protect from moisture by keeping bottle tightly closed. Dispense in a tight, light- resistant

container as defined in the USP, with a child-resistant closure (as required).

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

Manufactured by:

Zhejiang Huahai Pharmaceutical Co., Ltd.

Xunqiao, Linhai, Zhejiang 317024, China

Distributed by:

Solco Healthcare US, LLC

Cranbury, NJ 08512, USA

Rev: JUN2017

17412-01

Fosinopril Sodium Tablets  20 mg -- 90 tablets
(click image for full-size original)

Package/Label Display Panel – 40 mg

Container Label — 40 mg — 90 tablets

NDC 43547-388-09 Rx only

Fosinopril Sodium Tablets,USP

40 mg

90 Tablets

Each tablet contains:

40 mg of Fosinopril Sodium, USP.

Usual dosage: See package insert for full prescribing information.

Store at 20°C to 25°C (68°F to 77°F)

[See USP Controlled Room Temperature]

Protect from moisture by keeping bottle tightly closed. Dispense in a tight, light- resistant

container as defined in the USP, with a child-resistant closure (as required).

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

Manufactured by:

Zhejiang Huahai Pharmaceutical Co., Ltd.

Xunqiao, Linhai, Zhejiang 317024, China

Distributed by:

Solco Healthcare US, LLC

Cranbury, NJ 08512, USA

Rev: JUN2017

17414-01

Fosinopril Sodium Tablets  40 mg -- 90 tablets
(click image for full-size original)
FOSINOPRIL SODIUM
fosinopirl sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:43547-386
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FOSINOPRIL SODIUM (FOSINOPRILAT) FOSINOPRIL SODIUM 10 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
CELLULOSE, MICROCRYSTALLINE
CROSPOVIDONE
POVIDONE K29/32
SODIUM STEARYL FUMARATE
Product Characteristics
Color WHITE (white to off-white) Score 2 pieces
Shape CAPSULE Size 6mm
Flavor Imprint Code S;10
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:43547-386-09 90 TABLET in 1 BOTTLE None
2 NDC:43547-386-11 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA205670 10/01/2017
FOSINOPRIL SODIUM
fosinopril sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:43547-387
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FOSINOPRIL SODIUM (FOSINOPRILAT) FOSINOPRIL SODIUM 20 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
CROSPOVIDONE
POVIDONE K29/32
SODIUM STEARYL FUMARATE
CELLULOSE, MICROCRYSTALLINE
Product Characteristics
Color WHITE (white to off-white) Score no score
Shape ROUND Size 7mm
Flavor Imprint Code S;20
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:43547-387-09 90 TABLET in 1 BOTTLE None
2 NDC:43547-387-11 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA205670 10/01/2017
FOSINOPRIL SODIUM
fosinopril sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:43547-388
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FOSINOPRIL SODIUM (FOSINOPRILAT) FOSINOPRIL SODIUM 40 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
CROSPOVIDONE
POVIDONE K29/32
CELLULOSE, MICROCRYSTALLINE
SODIUM STEARYL FUMARATE
Product Characteristics
Color WHITE (white to off-white) Score no score
Shape ROUND Size 8mm
Flavor Imprint Code S;40
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:43547-388-09 90 TABLET in 1 BOTTLE None
2 NDC:43547-388-11 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA205670 10/01/2017
Labeler — Solco Healthcare LLC (828343017)

Revised: 12/2019 Solco Healthcare LLC

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