Glipizide
- Product NDC
- 82804-174
- 11-digit product format
- 828040174
- Labeler code
- 82804
- Product ID
- 82804-174_abe14fb1-e2fa-4c89-8007-fa4c18fd70a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA214874
- Marketing category
- ANDA
- Marketing start
- 2023-10-03
- 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 | 310490 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-174-30 | Glipizide | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 82804-174-90 | Glipizide | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82804-174 | GLIPIZIDE TABLET [PROFICIENT RX LP] | 2 | Current NDC, 2 package rows | 20250210_6427db20-6783-439f-8c2d-64d1a6fcb9fc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-174-30 | 82804017430 | 30 TABLET in 1 BOTTLE (82804-174-30) | 30 tablet | 2024-12-12 | No | No | Current |
| 82804-174-90 | 82804017490 | 90 TABLET in 1 BOTTLE (82804-174-90) | 90 tablet | 2025-01-20 | No | No | Current |