NDC 68084-342 – Topiramate

Topiramate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68084-342

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078235
Marketed since
April 10, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (1)

Package NDCDescriptionSince
68084-342-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-342-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-342-11)Apr 10, 2009

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