Clobetasol Propionate
- Product NDC
- 63739-064
- 11-digit product format
- 637390064
- Labeler code
- 63739
- Product ID
- 63739-064_8fd0f786-2366-4b80-b4b4-515e5cb32b81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clobetasol Propionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- McKesson Corporation
- Application
- ANDA209411
- Marketing category
- ANDA
- Marketing start
- 2017-08-21
- 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 |
|---|
| 63739-064-65 | 63739006465 | 1 TUBE in 1 CARTON (63739-064-65) > 15 g in 1 TUBE | 1 tube | 2021-07-02 | 0000-00-00 | No | No | Current |
| 63739-064-66 | 63739006466 | 1 TUBE in 1 CARTON (63739-064-66) > 30 g in 1 TUBE | 1 tube | 2021-07-02 | 0000-00-00 | No | No | Current |
| 63739-064-68 | 63739006468 | 1 TUBE in 1 CARTON (63739-064-68) > 60 g in 1 TUBE | 1 tube | 2021-07-02 | 0000-00-00 | No | No | Current |