DIPROLENE AF
- Product NDC
- 0085-0517
- 11-digit product format
- 000850517
- Labeler code
- 0085
- Product ID
- 0085-0517_18c66566-a68f-4926-bd37-2962ccad59c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- betamethasone dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Merck Sharp & Dohme Corp.
- Application
- NDA019555
- Marketing category
- NDA
- Marketing start
- 1987-04-27
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- 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 |
|---|
| 0085-0517-01 | 00085051701 | 1 TUBE in 1 BOX (0085-0517-01) > 15 g in 1 TUBE | 1 tube | 1987-04-27 | 0000-00-00 | No | No | Current |
| 0085-0517-04 | 00085051704 | 1 TUBE in 1 BOX (0085-0517-04) > 50 g in 1 TUBE | 1 tube | 1987-04-27 | 0000-00-00 | No | No | Current |