Baclofen (Page 2 of 2)

HOW SUPPLIED

Product: 50436-9022

NDC: 50436-9022-1 30 TABLET in a BOTTLE

NDC: 50436-9022-2 60 TABLET in a BOTTLE

NDC: 50436-9022-3 90 TABLET in a BOTTLE

NDC: 50436-9022-5 120 TABLET in a BOTTLE

BACLOFEN TABLET

Label Image
(click image for full-size original)
BACLOFEN
baclofen tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50436-9022(NDC:0172-4096)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BACLOFEN (BACLOFEN) BACLOFEN 10 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
SILICON DIOXIDE
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color WHITE (white to off white) Score 2 pieces
Shape ROUND Size 9mm
Flavor Imprint Code 4096;TV
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50436-9022-1 30 TABLET in 1 BOTTLE None
2 NDC:50436-9022-2 60 TABLET in 1 BOTTLE None
3 NDC:50436-9022-3 90 TABLET in 1 BOTTLE None
4 NDC:50436-9022-5 120 TABLET in 1 BOTTLE None
Image of Product
(click image for full-size original)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA072234 07/21/1988
Labeler — Unit Dose Services (831995316)
Establishment
Name Address ID/FEI Operations
Unit Dose Services 831995316 REPACK (50436-9022), RELABEL (50436-9022)

Revised: 03/2021 Unit Dose Services

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