Miglitol
- Product NDC
- 57664-685
- 11-digit product format
- 576640685
- Labeler code
- 57664
- Product ID
- 57664-685_75d82c09-b616-44a0-9ec3-a9cbd5b26ad4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Miglitol
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries Inc.
- Application
- ANDA203965
- Marketing category
- ANDA
- Marketing start
- 2016-01-04
- Marketing end
- 0000-00-00
- Substance
- MIGLITOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57664-685-88 | 57664068588 | 100 TABLET, COATED in 1 BOTTLE (57664-685-88) | 2016-04-21 | 0000-00-00 | No | No | Current |