Glipizide
- Product NDC
- 70518-4128
- 11-digit product format
- 705184128
- Labeler code
- 70518
- Product ID
- 70518-4128_4cab0981-453a-ba61-e063-6294a90a699b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2024-07-01
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glipizide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLIPIZIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X7WDT95N5C |
| Rxcui | 315107 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4128-0 | Glipizide | 30 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 30 | | 4 |
| 70518-4128-1 | Glipizide | 90 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-4128 | GLIPIZIDE (GLIPIZIDE) TABLET, EXTENDED RELEASE [REMEDYREPACK INC.] | 1 | Current NDC, 2 package rows | 20240703_667dd68a-d3e7-4b50-bd0a-d17783a090d5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4128-0 | 70518412800 | 30 in 1 BLISTER PACK | | | | Historical |
| 70518-4128-1 | 70518412801 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4128-1) | 2025-09-08 | No | No | Current |