Glipizide
- Product NDC
- 50090-0852
- 11-digit product format
- 500900852
- Labeler code
- 50090
- Product ID
- 50090-0852_d02e2a7a-7ed6-46f7-afbe-ec65142c82dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076467
- Marketing category
- ANDA
- Marketing start
- 2003-11-19
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [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 |
|---|
| 50090-0852-0 | GlipizideER | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 21 |
| 50090-0852-2 | GlipizideER | 90 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 90 | | 21 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0852 | GLIPIZIDE ER (GLIPIZIDE) TABLET, FILM COATED, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 21 | Legacy NDC, 2 package rows | 20210211_e8b4e73b-20ce-4d57-8214-04ad370b3390.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 |
|---|
| 50090-0852-0 | 50090085200 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-0852-0) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0852-2 | 50090085202 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-0852-2) | 2014-11-28 | 0000-00-00 | No | No | Current |