GLYBURIDE AND METFORMIN HYDROCHLORIDE
- Product NDC
- 61919-418
- 11-digit product format
- 619190418
- Labeler code
- 61919
- Product ID
- 61919-418_9c972291-71c8-b588-e053-2995a90ab657
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYBURIDE AND METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA077870
- Marketing category
- ANDA
- Marketing start
- 2015-12-03
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61919-418-60 | 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 |
|---|
| 61919-418 | GLYBURIDE AND METFORMIN HYDROCHLORIDE TABLET, FILM COATED [DIRECTRX] | 2 | Legacy NDC, 1 package rows | 20200131_26177ce8-8436-22c1-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-418-60 | 61919041860 | 60 TABLET, FILM COATED in 1 BOTTLE (61919-418-60) | 2015-12-03 | 0000-00-00 | No | No | Current |