Glipizide
- Product NDC
- 50090-4297
- 11-digit product format
- 500904297
- Labeler code
- 50090
- Product ID
- 50090-4297_1538f920-7243-4d77-8d7f-24be56351842
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4297 | GLIPIZIDE TABLET, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC | 20250417_29dc29b0-5d7d-4173-bc74-6375f7849a8e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4297-0 | 50090429700 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4297-0) | 2019-05-13 | 0000-00-00 | No | No | Current |
| 50090-4297-2 | 50090429702 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4297-2) | 2019-05-13 | 0000-00-00 | No | No | Current |