NDC 51672-4083 – Hydrocortisone Butyrate

Hydrocortisone Butyrate 1 mg/g · Ointment · Topical

Human Prescription Drug

Product NDC51672-4083

Product details

Brand name
Hydrocortisone Butyrate
Generic name
Hydrocortisone Butyrate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Ointment
Route
Topical
Marketing category
ANDA · ANDA076842
Marketed since
December 27, 2004
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Hydrocortisone Butyrate →

Package NDC codes (5)

Package NDCDescriptionSince
51672-4083-11 TUBE in 1 CARTON (51672-4083-1) / 15 g in 1 TUBEDec 27, 2004
51672-4083-21 TUBE in 1 CARTON (51672-4083-2) / 30 g in 1 TUBEDec 27, 2004
51672-4083-55 g in 1 TUBE (51672-4083-5)Dec 27, 2004
51672-4083-61 TUBE in 1 CARTON (51672-4083-6) / 45 g in 1 TUBEDec 27, 2004
51672-4083-71 TUBE in 1 CARTON (51672-4083-7) / 10 g in 1 TUBEDec 27, 2004

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