Glipizide
- Product NDC
- 70518-3898
- 11-digit product format
- 705183898
- Labeler code
- 70518
- Product ID
- 70518-3898_3f8dc598-35e8-cfa6-e063-6394a90a795e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2023-10-17
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glipizide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLIPIZIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X7WDT95N5C |
| Rxcui | 314006 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3898-0 | Glipizide | 90 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 90 | | 4 |
| 70518-3898-1 | Glipizide | 30 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3898 | GLIPIZIDE TABLET, EXTENDED RELEASE [REMEDYREPACK INC.] | 2 | Current NDC, 2 package rows | 20240404_0df8f606-97b3-463c-a132-338cf4630a71.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-3898-0 | 70518389800 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3898-0) | 2023-10-17 | No | No | Historical |
| 70518-3898-1 | 70518389801 | 30 in 1 BLISTER PACK | | | | Historical |