Betamethasone dipropionate
- Product NDC
- 50090-4679
- 11-digit product format
- 500904679
- Labeler code
- 50090
- Product ID
- 50090-4679_5a6ddf98-88a8-4181-a557-a4ed2ddb558a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betamethasone dipropionate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208885
- Marketing category
- ANDA
- Marketing start
- 2019-02-26
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4679 | BETAMETHASONE DIPROPIONATE CREAM [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC | 20231216_cd94c962-86cc-4553-8063-62f51ce9f2fd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4679-0 | 50090467900 | 1 TUBE in 1 CARTON (50090-4679-0) > 15 g in 1 TUBE | 1 tube | 2019-11-04 | 0000-00-00 | No | No | Current |