NDC 68382-004 – Topiramate

Topiramate 15 mg/1 · Capsule, Coated Pellets · Oral

Human Prescription Drug

Product NDC68382-004

Product details

Brand name
Topiramate
Generic name
Topiramate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule, Coated Pellets
Route
Oral
Marketing category
ANDA · ANDA078877
Marketed since
October 14, 2009
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Topiramate →

Package NDC codes (5)

Package NDCDescriptionSince
68382-004-01100 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-004-01)Oct 14, 2009
68382-004-05500 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-004-05)Oct 14, 2009
68382-004-101000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-004-10)Oct 14, 2009
68382-004-1460 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-004-14)Oct 14, 2009
68382-004-1690 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-004-16)Oct 14, 2009

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