Clobetasol Propionate
- Product NDC
- 68071-1600
- 11-digit product format
- 680711600
- Labeler code
- 68071
- Product ID
- 68071-1600_bb12089e-cb67-6345-e053-2a95a90a8a2a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA074089
- Marketing category
- ANDA
- Marketing start
- 2016-01-04
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1600-3 | 68071160003 | 30 g in 1 TUBE (68071-1600-3) | 30 g | 2019-04-04 | 0000-00-00 | No | No | Current |