Glyburide
- Product NDC
- 63187-667
- 11-digit product format
- 631870667
- Labeler code
- 63187
- Product ID
- 63187-667_d19e8583-285d-471e-a205-0c340584231b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090937
- Marketing category
- ANDA
- Marketing start
- 2010-10-05
- Substance
- GLYBURIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| SX6K58TVWC | GLYBURIDE | 10238-21-8 | GLYBURIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63187-667-30 | 63187066730 | 30 TABLET in 1 BOTTLE (63187-667-30) | 30 tablet | 2018-12-01 | No | No | Historical |
| 63187-667-60 | 63187066760 | 60 TABLET in 1 BOTTLE (63187-667-60) | 60 tablet | 2018-12-01 | No | No | Historical |
| 63187-667-90 | 63187066790 | 90 TABLET in 1 BOTTLE (63187-667-90) | 90 tablet | 2018-12-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| for oral use | Proficient Rx LP | 2019-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |