NDC 51672-1316 – Alclometasone Dipropionate
Alclometasone Dipropionate .5 mg/g · Ointment · Topical
Product NDC51672-1316
Product details
- Brand name
- Alclometasone Dipropionate
- Generic name
- Alclometasone dipropionate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Ointment
- Route
- Topical
- Marketing category
- ANDA · ANDA076730
- Marketed since
- July 29, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Alclometasone Dipropionate .5 mg/g
Uses, dosage, side effects and warnings for Alclometasone dipropionate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1316-1 | 1 TUBE in 1 CARTON (51672-1316-1) / 15 g in 1 TUBE | Jul 29, 2004 |
| 51672-1316-3 | 1 TUBE in 1 CARTON (51672-1316-3) / 60 g in 1 TUBE | Jul 29, 2004 |
| 51672-1316-5 | 5 g in 1 TUBE (51672-1316-5) | Jul 29, 2004 |
| 51672-1316-6 | 1 TUBE in 1 CARTON (51672-1316-6) / 45 g in 1 TUBE | Jul 29, 2004 |
Other Alclometasone dipropionate products
- 68462-299 Alclometasone Dipropionate .5 mg/g · Ointment · Glenmark Pharmaceuticals Inc., USA
- 0168-0263 Alclometasone Dipropionate .5 mg/g · Cream · E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
- 51672-1306 Alclometasone Dipropionate .5 mg/g · Cream · Sun Pharmaceutical Industries, Inc.