Clobetasol Propionate
- Product NDC
- 68071-2218
- 11-digit product format
- 680712218
- Labeler code
- 68071
- Product ID
- 68071-2218_d60ba55e-d200-351c-e053-2995a90a6cdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate Ointment USP, 0.05%
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA211295
- Marketing category
- ANDA
- Marketing start
- 2019-11-18
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68071-2218-5 | 68071221805 | 1 TUBE in 1 CARTON (68071-2218-5) > 15 g in 1 TUBE | 1 tube | 2020-07-17 | 0000-00-00 | No | No | Current |