NDC 0378-8200 – Ketoprofen

Ketoprofen 200 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC0378-8200

Product details

Brand name
Ketoprofen
Generic name
Ketoprofen
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA075679
Marketed since
September 4, 2003
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ketoprofen →

Package NDC codes (1)

Package NDCDescriptionSince
0378-8200-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0378-8200-01)Sep 4, 2003

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