Betamethasone Valerate
- Product NDC
- 0472-0371
- 11-digit product format
- 004720371
- Labeler code
- 0472
- Product ID
- 0472-0371_af0fcb94-9e3b-4b1f-8229-060508617b20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Valerate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA070051
- Marketing category
- ANDA
- Marketing start
- 1997-10-01
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE VALERATE
- Active strength
- 1 mg/g
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0472-0371-15 | 00472037115 | 1 TUBE in 1 CARTON (0472-0371-15) > 15 g in 1 TUBE | 1 tube | 1997-10-01 | 0000-00-00 | No | No | Current |
| 0472-0371-45 | 00472037145 | 1 TUBE in 1 CARTON (0472-0371-45) > 45 g in 1 TUBE | 1 tube | 1997-10-01 | 0000-00-00 | No | No | Current |