NDC 51672-1292 – Hydrocortisone Valerate
Hydrocortisone Valerate 2 mg/g · Ointment · Topical
Product NDC51672-1292
Product details
- Brand name
- Hydrocortisone Valerate
- Generic name
- Hydrocortisone Valerate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Ointment
- Route
- Topical
- Marketing category
- ANDA · ANDA075043
- Marketed since
- August 25, 1998
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Hydrocortisone Valerate 2 mg/g
Uses, dosage, side effects and warnings for Hydrocortisone Valerate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1292-1 | 1 TUBE in 1 CARTON (51672-1292-1) / 15 g in 1 TUBE | Aug 25, 1998 |
| 51672-1292-3 | 1 TUBE in 1 CARTON (51672-1292-3) / 60 g in 1 TUBE | Aug 25, 1998 |
| 51672-1292-6 | 1 TUBE in 1 CARTON (51672-1292-6) / 45 g in 1 TUBE | Aug 25, 1998 |
Other Hydrocortisone Valerate products
- 0713-0560 Hydrocortisone Valerate 2 mg/g · Ointment · Cosette Pharmaceuticals, Inc.
- 68462-836 Hydrocortisone Valerate 2 mg/g · Ointment · Glenmark Pharmaceuticals Inc., USA
- 0713-0720 Hydrocortisone Valerate 2 mg/g · Cream · Cosette Pharmaceuticals, Inc.
- 68180-954 Hydrocortisone Valerate 2 mg/g · Cream · Lupin Pharmaceuticals, Inc.
- 51672-1290 Hydrocortisone Valerate 2 mg/g · Cream · Sun Pharmaceutical Industries, Inc.