Lamotrigine (Page 12 of 12)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

71205-245-30
(click image for full-size original)
LAMOTRIGINE lamotrigine tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71205-245(NDC:29300-112)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LAMOTRIGINE (LAMOTRIGINE) LAMOTRIGINE 100 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
POVIDONE, UNSPECIFIED
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color WHITE Score 2 pieces
Shape TRIANGLE (Trigonal) Size 11mm
Flavor Imprint Code U;U;112
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71205-245-30 30 TABLET in 1 BOTTLE, PLASTIC None
2 NDC:71205-245-60 60 TABLET in 1 BOTTLE, PLASTIC None
3 NDC:71205-245-90 90 TABLET in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090170 11/01/2011
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (71205-245), RELABEL (71205-245)

Revised: 03/2020 Proficient Rx LP

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2022. All Rights Reserved.