BETAMETHASONE DIPROPIONATE
- Product NDC
- 52959-262
- 11-digit product format
- 529590262
- Labeler code
- 52959
- Product ID
- 52959-262_82fd507e-927c-70e1-e053-2a91aa0ac903
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BETAMETHASONE DIPROPIONATE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA071012
- Marketing category
- ANDA
- Marketing start
- 2015-01-04
- 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
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 |
|---|
| 52959-262-00 | BETAMETHASONE DIPROPIONATE | 45 g in 1 TUBE | OINTMENT | 45 | | 1 |
| 52959-262-15 | BETAMETHASONE DIPROPIONATE | 15 g in 1 TUBE | OINTMENT | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-262 | BETAMETHASONE DIPROPIONATE OINTMENT [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 2 package rows | 20190301_82fd507e-927b-70e1-e053-2a91aa0ac903.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52959-262-00 | 52959026200 | 45 g in 1 TUBE (52959-262-00) | 45 g | 2015-01-04 | 0000-00-00 | No | No | Current |
| 52959-262-15 | 52959026215 | 15 g in 1 TUBE (52959-262-15) | 15 g | 2015-01-04 | 0000-00-00 | No | No | Current |