Betamethasone Dipropionate
- Product NDC
- 68788-0382
- 11-digit product format
- 687880382
- Labeler code
- 68788
- Product ID
- 68788-0382_d37c2cdc-b6ac-4d08-b63b-7aa96734d6ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- OINTMENT, AUGMENTED
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074304
- Marketing category
- ANDA
- Marketing start
- 2013-03-19
- 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 |
|---|
| 68788-0382-1 | 68788038201 | 1 TUBE in 1 CARTON (68788-0382-1) > 15 g in 1 TUBE | 1 tube | 2013-03-19 | 0000-00-00 | No | No | Current |