Betamethasone Dipropionate
- Product NDC
- 68788-9804
- 11-digit product format
- 687889804
- Labeler code
- 68788
- Product ID
- 68788-9804_327f8381-adc5-44e6-829b-e1a156fdc94a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078930
- Marketing category
- ANDA
- Marketing start
- 2012-04-23
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- 1 mg/g
- 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 |
|---|
| 68788-9804-1 | 68788980401 | 15 g in 1 TUBE (68788-9804-1) | 15 g | 2012-04-23 | 0000-00-00 | No | No | Current |