Betamethasone Dipropionate
- Product NDC
- 0713-0728
- 11-digit product format
- 007130728
- Labeler code
- 0713
- Product ID
- 0713-0728_dde30fad-5417-07e5-e053-2a95a90a8883
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA071467
- Marketing category
- ANDA
- Marketing start
- 1987-08-10
- Marketing end
- 2023-01-31
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0713-0728-53 | 00713072853 | 1 BOTTLE in 1 CARTON (0713-0728-53) > 60 mL in 1 BOTTLE | 1 bottle | 2018-08-24 | 0000-00-00 | No | No | Current |