Alprazolam (Page 10 of 10)

PRINCIPAL DISPLAY PANEL — 0.5 mg Tablet Bottle Label

NDC 71205-284-30

CIV

Alprazolam
Tablets, USP
0.5 mg

PHARMACIST: Dispense the
accompanying Medication Guide to each patient.

Rx Only

71205-284-30
(click image for full-size original)
ALPRAZOLAM alprazolam tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71205-284(NDC:51991-705)
Route of Administration ORAL DEA Schedule CIV
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alprazolam (alprazolam) Alprazolam 0.5 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
FD&C YELLOW NO. 6
Product Characteristics
Color ORANGE (light orange to orange) Score 2 pieces
Shape OVAL Size 9mm
Flavor Imprint Code B705
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71205-284-30 30 TABLET in 1 BOTTLE None
2 NDC:71205-284-60 60 TABLET in 1 BOTTLE None
3 NDC:71205-284-90 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA207507 07/09/2018
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (71205-284), RELABEL (71205-284)

Revised: 01/2023 Proficient Rx LP

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