GLYBURIDE AND METFORMIN HYDROCHLORIDE
- Product NDC
- 55111-696
- 11-digit product format
- 551110696
- Labeler code
- 55111
- Product ID
- 55111-696_279b92ac-8e31-4b04-8983-6f161f5b709c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYBURIDE AND METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Limited
- Application
- ANDA079009
- Marketing category
- ANDA
- Marketing start
- 2009-06-30
- 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
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 55111-696-01 | GLYBURIDE AND METFORMIN HYDROCHLORIDE | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 55111-696-05 | GLYBURIDE AND METFORMIN HYDROCHLORIDE | 500 in 1 BOTTLE | TABLET | 500 | | 2 |
| 55111-696-10 | GLYBURIDE AND METFORMIN HYDROCHLORIDE | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55111-696 | GLYBURIDE AND METFORMIN HYDROCHLORIDE TABLET [DR. REDDY'S LABORATORIES LIMITED] | 2 | Legacy NDC, 3 package rows | 20090701_89245260-c470-4a4c-8ef6-12598dc28e4c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55111-696-01 | 55111069601 | 100 in 1 BOTTLE | Historical |
| 55111-696-05 | 55111069605 | 500 in 1 BOTTLE | Historical |
| 55111-696-10 | 55111069610 | 1000 in 1 BOTTLE | Historical |