NDC 69097-817 – Topiramate

Topiramate 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69097-817

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA079162
Marketed since
July 22, 2016
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (3)

Package NDCDescriptionSince
69097-817-0360 TABLET in 1 BOTTLE (69097-817-03)Jul 22, 2016
69097-817-12500 TABLET in 1 BOTTLE (69097-817-12)Jul 22, 2016
69097-817-151000 TABLET in 1 BOTTLE (69097-817-15)Jul 22, 2016

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