Alprazolam (Page 10 of 10)

Principal Display Panel

NDC: 51655-266-52

Label
(click image for full-size original)
ALPRAZOLAM alprazolam tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-266(NDC:51991-704)
Route of Administration ORAL DEA Schedule CIV
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALPRAZOLAM (ALPRAZOLAM) ALPRAZOLAM 0.25 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MICROCRYSTALLINE CELLULOSE
SODIUM STARCH GLYCOLATE TYPE A CORN
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
SODIUM LAURYL SULFATE
MAGNESIUM STEARATE
Product Characteristics
Color white (white to off-white) Score 2 pieces
Shape OVAL Size 9mm
Flavor Imprint Code B704
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51655-266-52 30 TABLET in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA207507 03/07/2019
Labeler — Northwind Pharmaceuticals (036986393)
Registrant — Northwind Pharmaceuticals (036986393)
Establishment
Name Address ID/FEI Operations
EPM Packaging Inc 079124340 repack (51655-266)

Revised: 08/2020 Northwind Pharmaceuticals

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