Betamethasone Dipropionate
- Product NDC
- 50090-7517
- 11-digit product format
- 500907517
- Labeler code
- 50090
- Product ID
- 50090-7517_3140f140-758c-41a6-83e2-8cb9be901863
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- betamethasone dipropionate
- Dosage form
- OINTMENT, AUGMENTED
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075373
- Marketing category
- ANDA
- Marketing start
- 1999-06-22
- Substance
- BETAMETHASONE DIPROPIONATE
- Active strength
- .5 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Betamethasone Dipropionate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BETAMETHASONE DIPROPIONATE | .5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 826Y60901U |
| Rxcui | 848180 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7517-0 | Betamethasone Dipropionate | 50 g in 1 TUBE | OINTMENT, AUGMENTED | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7517 | BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 1 package rows | 20250316_018fcec3-bfb4-451c-9b54-d1fd389c2a44.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7517-0 | 50090751700 | 50 g in 1 TUBE (50090-7517-0) | 50 g | 2025-03-11 | No | No | Historical |