Glipizide
- Product NDC
- 70518-2624
- 11-digit product format
- 705182624
- Labeler code
- 70518
- Product ID
- 70518-2624_d6ba7b6e-0bb5-4f5a-e053-2995a90af94c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2020-03-12
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2624 | GLIPIZIDE TABLET, EXTENDED RELEASE [REMEDYREPACK INC.] | 6 | Legacy NDC | 20240306_cdebc7b3-2d2f-4022-8f36-ce9a4eb27206.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2624-0 | 70518262400 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2624-0) | 2020-03-12 | 0000-00-00 | No | No | Current |
| 70518-2624-1 | 70518262401 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2624-1) | 2020-04-17 | 0000-00-00 | No | No | Current |
| 70518-2624-2 | 70518262402 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2624-2) | 2020-11-18 | 0000-00-00 | No | No | Current |