Glipizide and Metformin Hydrochloride
- Product NDC
- 50090-1080
- 11-digit product format
- 500901080
- Labeler code
- 50090
- Product ID
- 50090-1080_58531850-5277-438c-a988-b05eaacba6a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077270
- Marketing category
- ANDA
- Marketing start
- 2005-10-28
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE; 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
- 2022-12-31
- 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 |
|---|
| 50090-1080-0 | Glipizide and Metformin Hydrochloride | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1080 | GLIPIZIDE AND METFORMIN HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 12 | Legacy NDC, 1 package rows | 20210116_ae9a4e65-4613-42cf-a310-0fce9f1f93e8.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 |
|---|
| 50090-1080-0 | 50090108000 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-1080-0) | 2014-11-28 | 0000-00-00 | No | No | Current |