Glimepiride
- Product NDC
- 60760-248
- 11-digit product format
- 607600248
- Labeler code
- 60760
- Product ID
- 60760-248_f06e9242-c9fa-f3c9-e053-2a95a90a276a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary
- Application
- ANDA078181
- Marketing category
- ANDA
- Marketing start
- 2017-12-26
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-248 | GLIMEPIRIDE TABLET [ST. MARY’S MEDICAL PARK PHARMACY] | 4 | Legacy NDC | 20221223_6142a6db-6dae-507c-e053-2991aa0a0923.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-248-90 | 60760024890 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-248-90) | 90 tablet | 2017-12-26 | 0000-00-00 | No | No | Current |