Glipizide
- Product NDC
- 63187-255
- 11-digit product format
- 631870255
- Labeler code
- 63187
- Product ID
- 63187-255_aaf7b64f-f795-40ea-85be-d0eb6feb4f78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA074550
- Marketing category
- ANDA
- Marketing start
- 2011-03-01
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-255 | GLIPIZIDE TABLET [PROFICIENT RX LP] | 5 | Legacy NDC | 20210116_2e51d1ae-a486-4d7a-b5ee-2324c8c42fb2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-255-30 | 63187025530 | 30 TABLET in 1 BOTTLE (63187-255-30) | 30 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 63187-255-60 | 63187025560 | 60 TABLET in 1 BOTTLE (63187-255-60) | 60 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 63187-255-90 | 63187025590 | 90 TABLET in 1 BOTTLE (63187-255-90) | 90 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |