Glimepiride
- Product NDC
- 55700-722
- 11-digit product format
- 557000722
- Labeler code
- 55700
- Product ID
- 55700-722_1dc2b175-4ac3-42b8-9f69-1a7357ee5f45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA078181
- Marketing category
- ANDA
- Marketing start
- 2019-01-25
- Marketing end
- 0000-00-00
- Substance
- GLIMEPIRIDE
- Active strength
- 4 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-722-30 | 55700072230 | 30 TABLET in 1 BOTTLE (55700-722-30) | 30 tablet | 2019-01-25 | 0000-00-00 | No | No | Current |