GLIPIZIDE
- Product NDC
- 61919-476
- 11-digit product format
- 619190476
- Labeler code
- 61919
- Product ID
- 61919-476_9c9424d4-4270-110f-e053-2995a90ac6c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLIPIZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA074550
- Marketing category
- ANDA
- Marketing start
- 2017-02-24
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-476-30 | GLIPIZIDE | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-476 | GLIPIZIDE TABLET [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20200121_494ce357-e390-65e8-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-476-30 | 61919047630 | 30 TABLET in 1 BOTTLE (61919-476-30) | 30 tablet | 2017-02-24 | 0000-00-00 | No | No | Current |