Glipizide
- Product NDC
- 50090-2915
- 11-digit product format
- 500902915
- Labeler code
- 50090
- Product ID
- 50090-2915_da010396-c7e5-4fbd-b8b1-055d18813e89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076159
- Marketing category
- ANDA
- Marketing start
- 2016-12-21
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [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 |
|---|
| 50090-2915-0 | Glipizide | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 7 |
| 50090-2915-1 | Glipizide | 60 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 60 | | 7 |
| 50090-2915-2 | Glipizide | 90 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 90 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2915 | GLIPIZIDE TABLET, FILM COATED, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC, 3 package rows | 20200122_999d353d-ef88-45fb-8df9-572c0d2bb1e2.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 |
|---|
| 50090-2915-0 | 50090291500 | 30 in 1 BOTTLE | | | | | Historical |
| 50090-2915-1 | 50090291501 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-2915-1) | 2018-09-25 | 0000-00-00 | No | No | Current |
| 50090-2915-2 | 50090291502 | 90 in 1 BOTTLE | | | | | Historical |