GLYBURIDE
- Product NDC
- 70518-1201
- 11-digit product format
- 705181201
- Labeler code
- 70518
- Product ID
- 70518-1201_f1d6b207-24ee-031f-e053-2a95a90a5d3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYBURIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090937
- Marketing category
- ANDA
- Marketing start
- 2018-05-15
- Marketing end
- 0000-00-00
- Substance
- GLYBURIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1201-0 | 70518120100 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-1201-0) | 100 tablet | 2018-05-15 | 0000-00-00 | No | No | Current |
| 70518-1201-1 | 70518120101 | 360 TABLET in 1 BOTTLE, PLASTIC (70518-1201-1) | 360 tablet | 2019-11-22 | 0000-00-00 | No | No | Current |