Glyburide and Metformin Hydrochloride
- Product NDC
- 70934-570
- 11-digit product format
- 709340570
- Labeler code
- 70934
- Product ID
- 70934-570_abfe077e-c4b8-568e-e053-2a95a90a1b81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA077870
- Marketing category
- ANDA
- Marketing start
- 2020-02-25
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-570-90 | 70934057090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-570-90) | 2020-02-25 | 0000-00-00 | No | No | Current |