Betamethasone Valerate
- Product NDC
- 21695-586
- 11-digit product format
- 216950586
- Labeler code
- 21695
- Product ID
- 21695-586_eeb337ba-0d7e-42cd-840a-78783b5688d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- betamethasone valerate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA018865
- Marketing category
- ANDA
- Marketing start
- 2009-10-23
- Marketing end
- 0000-00-00
- Substance
- BETAMETHASONE VALERATE
- Active strength
- 1 mg/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-586-45 | Betamethasone Valerate | 45 g in 1 TUBE | OINTMENT | 45 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-586 | BETAMETHASONE VALERATE OINTMENT [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20101119_eeb337ba-0d7e-42cd-840a-78783b5688d7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 21695-586-45 | 21695058645 | 45 g in 1 TUBE | 45 g | Historical |