Glipizide
- Product NDC
- 60687-480
- 11-digit product format
- 606870480
- Labeler code
- 60687
- Product ID
- 60687-480_e33ad6df-cdd9-75f0-e053-2a95a90a4dd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2022-03-04
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 3 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 |
|---|
| 60687-480 | GLIPIZIDE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING] | 4 | Legacy NDC | 20230804_9cc4b247-d211-4b5e-ba2c-b68848631c2a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-480-21 | 60687048021 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-480-21) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-480-11) | 30 blister pack | 2020-01-20 | 0000-00-00 | No | No | Current |