Clobetasol Propionate
- Product NDC
- 70518-2068
- 11-digit product format
- 705182068
- Labeler code
- 70518
- Product ID
- 70518-2068_dacee119-10cc-67e4-e053-2a95a90a1bca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clobetasol propionate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200302
- Marketing category
- ANDA
- Marketing start
- 2019-05-08
- Marketing end
- 0000-00-00
- Substance
- CLOBETASOL PROPIONATE
- Active strength
- 1 mg/mL
- 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 |
|---|
| 70518-2068-0 | 70518206800 | 1 BOTTLE in 1 CARTON (70518-2068-0) > 118 mL in 1 BOTTLE | 1 bottle | 2019-05-08 | 0000-00-00 | No | No | Current |