Betamethasone Dipropionate
- Product NDC
- 50090-4038
- 11-digit product format
- 500904038
- Labeler code
- 50090
- Product ID
- 50090-4038_5be215bf-2170-4274-ba81-285cadfcfbf5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA073552
- Marketing category
- ANDA
- Marketing start
- 1992-04-30
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE DIPROPIONATE
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4038-0 | 50090403800 | 1 TUBE in 1 CARTON (50090-4038-0) > 45 g in 1 TUBE | 1 tube | 2019-01-09 | 0000-00-00 | No | No | Current |