NDC 71205-936 – Miglitol
Miglitol 50 mg/1 · Tablet, Coated · Oral
Product NDC71205-936
Product details
- Brand name
- Miglitol
- Generic name
- Miglitol
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203965
- Marketed since
- January 15, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Glucosidase Inhibitor
Active ingredients
- Miglitol 50 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71205-936-00 | 100 TABLET, COATED in 1 BOTTLE (71205-936-00) | Mar 1, 2021 |
| 71205-936-30 | 30 TABLET, COATED in 1 BOTTLE (71205-936-30) | Mar 1, 2021 |
| 71205-936-60 | 60 TABLET, COATED in 1 BOTTLE (71205-936-60) | Mar 1, 2021 |
| 71205-936-90 | 90 TABLET, COATED in 1 BOTTLE (71205-936-90) | Mar 1, 2021 |
Other Miglitol products
- 71205-935 Miglitol 25 mg/1 · Tablet, Coated · Proficient Rx LP
- 71205-937 Miglitol 100 mg/1 · Tablet, Coated · Proficient Rx LP
- 69367-303 Miglitol 25 mg/1 · Tablet, Coated · Westminster Pharmaceuticals, LLC
- 69367-304 Miglitol 50 mg/1 · Tablet, Coated · Westminster Pharmaceuticals, LLC
- 69367-305 Miglitol 100 mg/1 · Tablet, Coated · Westminster Pharmaceuticals, LLC