Lamivudine (Page 7 of 7)

NDC 54838-566 -70

Lamivudine Oral Solution, USP

10 mg per 1 mL

Alcohol (5% v/v)

Rx Only

240 mL (8 ounces)

Lannett

bottle label 240 mL (8 ounces)
(click image for full-size original)

LAMIVUDINE lamivudine solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:54838-566
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LAMIVUDINE (LAMIVUDINE) LAMIVUDINE 10 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
EDETATE DISODIUM
ANHYDROUS CITRIC ACID
METHYLPARABEN
PROPYLPARABEN
SODIUM CITRATE
SUCROSE
WATER
PROPYLENE GLYCOL
Product Characteristics
Color Score
Shape Size
Flavor STRAWBERRY (artificial strawberry) Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:54838-566-70 240 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203564 10/31/2014
Labeler — Lannett Company, Inc. (161630033)
Establishment
Name Address ID/FEI Operations
Lannett Company, Inc. 161630033 ANALYSIS (54838-566), LABEL (54838-566), MANUFACTURE (54838-566), PACK (54838-566)

Revised: 01/2021 Lannett Company, Inc.

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