NDC 51672-1310 – Betamethasone Dipropionate

Betamethasone Dipropionate .5 mg/g · Cream, Augmented · Topical

Human Prescription Drug

Product NDC51672-1310

Product details

Brand name
Betamethasone Dipropionate
Generic name
Betamethasone Dipropionate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream, Augmented
Route
Topical
Marketing category
ANDA · ANDA076543
Marketed since
December 9, 2003
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Betamethasone Dipropionate →

Package NDC codes (3)

Package NDCDescriptionSince
51672-1310-11 TUBE in 1 CARTON (51672-1310-1) / 15 g in 1 TUBEDec 9, 2003
51672-1310-21 TUBE in 1 CARTON (51672-1310-2) / 30 g in 1 TUBEDec 9, 2003
51672-1310-31 TUBE in 1 CARTON (51672-1310-3) / 50 g in 1 TUBEDec 9, 2003

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