Betamethasone Dipropionate
- Product NDC
- 68071-1657
- 11-digit product format
- 680711657
- Labeler code
- 68071
- Product ID
- 68071-1657_bb1266f5-d751-9543-e053-2995a90ac1a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078930
- Marketing category
- ANDA
- Marketing start
- 2008-09-23
- 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 |
|---|
| 68071-1657-5 | 68071165705 | 15 g in 1 BOX (68071-1657-5) | 15 g | 2017-07-12 | 0000-00-00 | No | No | Current |