Betamethasone Dipropionate
- Product NDC
- 50090-4136
- 11-digit product format
- 500904136
- Labeler code
- 50090
- Product ID
- 50090-4136_f49d666b-6b9a-413a-bb61-c26dc0b7106e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone Dipropionate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- NDA019141
- Marketing category
- NDA
- Marketing start
- 1984-09-04
- 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
- 2020-12-31
- 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 |
|---|
| 50090-4136-0 | 50090413600 | 1 TUBE in 1 CARTON (50090-4136-0) > 45 g in 1 TUBE | 1 tube | 2019-02-11 | 0000-00-00 | No | No | Current |