Halobetasol Propionate
- Product NDC
- 0713-0639
- 11-digit product format
- 007130639
- Labeler code
- 0713
- Product ID
- 0713-0639_586c3345-52af-4f44-81d0-96429f1444ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Halobetasol Propionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA077721
- Marketing category
- ANDA
- Marketing start
- 2016-09-21
- Marketing end
- 0000-00-00
- Substance
- HALOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0713-0639-15 | 00713063915 | 1 TUBE in 1 CARTON (0713-0639-15) > 15 g in 1 TUBE | 1 tube | 2016-09-21 | 0000-00-00 | No | No | Current |
| 0713-0639-86 | 00713063986 | 1 TUBE in 1 CARTON (0713-0639-86) > 50 g in 1 TUBE | 1 tube | 2016-09-21 | 0000-00-00 | No | No | Current |