Betamethasone Dipropionate
- Product NDC
- 61748-480
- 11-digit product format
- 617480480
- Labeler code
- 61748
- Product ID
- 61748-480_935b71b9-1535-47bd-81cd-fdea9b2b03c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- LOTION, AUGMENTED
- Route
- TOPICAL
- Labeler
- Versapharm Incorporated
- Application
- ANDA208849
- Marketing category
- ANDA
- Marketing start
- 2019-11-15
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61748-480-30 | 61748048030 | 1 BOTTLE, PLASTIC in 1 CARTON (61748-480-30) > 30 mL in 1 BOTTLE, PLASTIC | 2019-11-15 | 0000-00-00 | No | No | Current |
| 61748-480-60 | 61748048060 | 1 BOTTLE, PLASTIC in 1 CARTON (61748-480-60) > 60 mL in 1 BOTTLE, PLASTIC | 2019-11-15 | 0000-00-00 | No | No | Current |