NDC 51672-4083 – Hydrocortisone Butyrate
Hydrocortisone Butyrate 1 mg/g · Ointment · Topical
Product NDC51672-4083
Product details
- Brand name
- Hydrocortisone Butyrate
- Generic name
- Hydrocortisone Butyrate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Ointment
- Route
- Topical
- Marketing category
- ANDA · ANDA076842
- Marketed since
- December 27, 2004
- Listing expires
- December 31, 2027
- Pharmacologic class
- Corticosteroid
Active ingredients
- Hydrocortisone Butyrate 1 mg/g
Uses, dosage, side effects and warnings for Hydrocortisone Butyrate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4083-1 | 1 TUBE in 1 CARTON (51672-4083-1) / 15 g in 1 TUBE | Dec 27, 2004 |
| 51672-4083-2 | 1 TUBE in 1 CARTON (51672-4083-2) / 30 g in 1 TUBE | Dec 27, 2004 |
| 51672-4083-5 | 5 g in 1 TUBE (51672-4083-5) | Dec 27, 2004 |
| 51672-4083-6 | 1 TUBE in 1 CARTON (51672-4083-6) / 45 g in 1 TUBE | Dec 27, 2004 |
| 51672-4083-7 | 1 TUBE in 1 CARTON (51672-4083-7) / 10 g in 1 TUBE | Dec 27, 2004 |
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