Glipizide
- Product NDC
- 70771-1099
- 11-digit product format
- 707711099
- Labeler code
- 70771
- Product ID
- 70771-1099_dcd3fc9f-03e4-40da-b468-ec8710c648e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA203499
- Marketing category
- ANDA
- Marketing start
- 2018-07-25
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1099-0 | 70771109900 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1099-0) | | 2018-07-25 | 0000-00-00 | No | No | Current |
| 70771-1099-1 | 70771109901 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1099-1) | | 2018-07-25 | 0000-00-00 | No | No | Current |
| 70771-1099-3 | 70771109903 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1099-3) | | 2018-07-25 | 0000-00-00 | No | No | Current |
| 70771-1099-4 | 70771109904 | 10 BLISTER PACK in 1 CARTON (70771-1099-4) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70771-1099-2) | 10 blister pack | 2018-07-25 | 0000-00-00 | No | No | Current |
| 70771-1099-5 | 70771109905 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1099-5) | | 2018-07-25 | 0000-00-00 | No | No | Current |
| 70771-1099-6 | 70771109906 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1099-6) | | 2018-07-25 | 0000-00-00 | No | No | Current |
| 70771-1099-9 | 70771109909 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1099-9) | | 2018-07-25 | 0000-00-00 | No | No | Current |