NDC 71335-2318 – Topiramate

Topiramate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2318

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090162
Marketed since
July 1, 2013
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2318-160 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-1)Jan 2, 2024
71335-2318-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-2)Jan 2, 2024
71335-2318-390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-3)Jan 2, 2024
71335-2318-4120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-4)Jan 2, 2024
71335-2318-550 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-5)Jan 2, 2024
71335-2318-614 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-6)Jan 2, 2024
71335-2318-745 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-7)Jan 2, 2024
71335-2318-87 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2318-8)Jan 2, 2024

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