Glyburide and Metformin Hydrochloride
- Product NDC
- 50436-0024
- 11-digit product format
- 504360024
- Labeler code
- 50436
- Product ID
- 50436-0024_90b260cb-f501-4486-a5fe-6822d76e1f80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077870
- Marketing category
- ANDA
- Marketing start
- 2007-11-14
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 3 mg/1; mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
- 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 |
|---|
| 50436-0024-2 | Glyburide and Metformin Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0024 | GLYBURIDE AND METFORMIN HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20180929_ae88900e-8146-4b3d-b62e-8ea836dfdbd6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0024-2 | 50436002402 | 60 in 1 BOTTLE | Historical |