NDC 51672-1310 – Betamethasone Dipropionate
Betamethasone Dipropionate .5 mg/g · Cream, Augmented · Topical
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
- Betamethasone Dipropionate .5 mg/g
Uses, dosage, side effects and warnings for Betamethasone Dipropionate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1310-1 | 1 TUBE in 1 CARTON (51672-1310-1) / 15 g in 1 TUBE | Dec 9, 2003 |
| 51672-1310-2 | 1 TUBE in 1 CARTON (51672-1310-2) / 30 g in 1 TUBE | Dec 9, 2003 |
| 51672-1310-3 | 1 TUBE in 1 CARTON (51672-1310-3) / 50 g in 1 TUBE | Dec 9, 2003 |
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