Glipizide
- Product NDC
- 70518-3896
- 11-digit product format
- 705183896
- Labeler code
- 70518
- Product ID
- 70518-3896_4b91b1e5-466b-2a72-e063-6294a90a9e5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203499
- Marketing category
- ANDA
- Marketing start
- 2023-10-17
- 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 |
|---|
| 70518-3896-0 | Glipizide | 30 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3896 | GLIPIZIDE TABLET, EXTENDED RELEASE [REMEDYREPACK INC.] | 3 | Current NDC, 1 package rows | 20250406_e593552f-9817-4cb5-b491-31ea57dea4b8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-3896-0 | 70518389600 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3896-0) | 2023-10-17 | No | No | Historical |