NDC 0555-0635 – Danazol

Danazol 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC0555-0635

Product details

Brand name
Danazol
Generic name
Danazol
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA074582
Marketed since
August 9, 1996
Listing expires
December 31, 2026
Pharmacologic class
Androgen

Active ingredients

Uses, dosage, side effects and warnings for Danazol →

Package NDC codes (2)

Package NDCDescriptionSince
0555-0635-02100 CAPSULE in 1 BOTTLE (0555-0635-02)Aug 9, 1996
0555-0635-0960 CAPSULE in 1 BOTTLE (0555-0635-09)Aug 9, 1996

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