NDC 71205-862 – Danazol

Danazol 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71205-862

Product details

Brand name
Danazol
Generic name
Danazol
Labeler
Proficient Rx LP
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077246
Marketed since
September 28, 2005
Listing expires
December 31, 2026
Pharmacologic class
Androgen

Active ingredients

Uses, dosage, side effects and warnings for Danazol →

Package NDC codes (6)

Package NDCDescriptionSince
71205-862-00100 CAPSULE in 1 BOTTLE (71205-862-00)Apr 1, 2022
71205-862-3030 CAPSULE in 1 BOTTLE (71205-862-30)Apr 1, 2022
71205-862-55500 CAPSULE in 1 BOTTLE (71205-862-55)Apr 1, 2022
71205-862-6060 CAPSULE in 1 BOTTLE (71205-862-60)Apr 1, 2022
71205-862-72120 CAPSULE in 1 BOTTLE (71205-862-72)Apr 1, 2022
71205-862-9090 CAPSULE in 1 BOTTLE (71205-862-90)Apr 1, 2022

Other Danazol products