Clotrimazole and Betamethasone Dipropionate
- Product NDC
- 0168-0370
- 11-digit product format
- 001680370
- Labeler code
- 0168
- Product ID
- 0168-0370_9959fe30-5f39-44ca-ad36-907fcc204ced
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clotrimazole and Betamethasone Dipropionate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
- Application
- ANDA076516
- Marketing category
- ANDA
- Marketing start
- 2005-06-16
- Marketing end
- 0000-00-00
- Substance
- CLOTRIMAZOLE; BETAMETHASONE DIPROPIONATE
- Active strength
- 10 mg/mL; mg/mL
- Pharmacologic classes
- Azole Antifungal [EPC],Azoles [CS],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0168-0370-30 | 00168037030 | 30 mL in 1 BOTTLE (0168-0370-30) | 30 ml | 2005-06-16 | 0000-00-00 | No | No | Current |