Glipizide
- Product NDC
- 50090-6849
- 11-digit product format
- 500906849
- Labeler code
- 50090
- Product ID
- 50090-6849_6fd6db61-c772-4909-a782-2f7dcd296c89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203499
- Marketing category
- ANDA
- Marketing start
- 2018-12-01
- Substance
- GLIPIZIDE
- Active strength
- 10 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 | 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 |
|---|
| 50090-6849-0 | Glipizide | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6849 | GLIPIZIDE TABLET, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 1 package rows | 20231205_15308fc4-11e3-4cd5-8f04-ab8e3433cc7d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6849-0 | 50090684900 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6849-0) | 2023-11-29 | No | No | Current |