Glimepiride
- Product NDC
- 68001-179
- 11-digit product format
- 680010179
- Labeler code
- 68001
- Product ID
- 68001-179_eff41a95-d73d-ed0a-e053-2995a90acfc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA078181
- Marketing category
- ANDA
- Marketing start
- 2014-02-26
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68001-179 | GLIMEPIRIDE TABLET [BLUEPOINT LABORATORIES] | 13 | Legacy NDC | 20240223_d162c78f-d176-4150-8dda-2c4a5d215014.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-179-00 | 68001017900 | 100 TABLET in 1 BOTTLE (68001-179-00) | 100 tablet | 2014-02-26 | 0000-00-00 | No | No | Current |
| 68001-179-03 | 68001017903 | 500 TABLET in 1 BOTTLE (68001-179-03) | 500 tablet | 2014-02-26 | 0000-00-00 | No | No | Current |