Halobetasol Propionate
- Product NDC
- 63739-998
- 11-digit product format
- 637390998
- Labeler code
- 63739
- Product ID
- 63739-998_de8d7dff-2dda-4bf2-afea-1d31b4038ec4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- halobetasol propionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- McKesson Corporation
- Application
- ANDA209978
- Marketing category
- ANDA
- Marketing start
- 2020-03-11
- 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
- 2021-12-31
- 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 |
|---|
| 63739-998-67 | 63739099867 | 1 TUBE in 1 CARTON (63739-998-67) > 50 g in 1 TUBE | 1 tube | 2020-03-11 | 0000-00-00 | No | No | Current |