NDC 51672-1340 – Betamethasone Dipropionate

Betamethasone Dipropionate .5 mg/mL · Lotion, Augmented · Topical

Human Prescription Drug

Product NDC51672-1340

Product details

Brand name
Betamethasone Dipropionate
Generic name
Betamethasone Dipropionate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Lotion, Augmented
Route
Topical
Marketing category
ANDA · ANDA077477
Marketed since
May 21, 2007
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
51672-1340-31 BOTTLE in 1 CARTON (51672-1340-3) / 30 mL in 1 BOTTLEMay 21, 2007
51672-1340-41 BOTTLE in 1 CARTON (51672-1340-4) / 60 mL in 1 BOTTLEMay 21, 2007

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