Glyburide and Metformin Hydrochloride
- Product NDC
- 50090-0888
- 11-digit product format
- 500900888
- Labeler code
- 50090
- Product ID
- 50090-0888_c1c4494b-ee2c-48b5-8c4b-5351eab42e0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077870
- Marketing category
- ANDA
- Marketing start
- 2007-11-14
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0888 | GLYBURIDE AND METFORMIN HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC | 20230208_94608538-eabf-4181-b3ff-95cf65af729c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0888-0 | 50090088800 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-0888-0) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0888-1 | 50090088801 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-0888-1) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0888-2 | 50090088802 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-0888-2) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0888-3 | 50090088803 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-0888-3) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0888-4 | 50090088804 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-0888-4) | 2014-11-28 | 0000-00-00 | No | No | Current |