NDC 43393-001 – Mifepristone
Mifepristone 200 mg/1 · Tablet · Oral
Product NDC43393-001
Product details
- Brand name
- Mifepristone
- Generic name
- Mifepristone
- Labeler
- GenBioPro, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091178
- Marketed since
- May 1, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Progestin Antagonist
Active ingredients
- Mifepristone 200 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 43393-001-06 | 6 CARTON in 1 PACKAGE (43393-001-06) / 1 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK (43393-001-01) | May 1, 2019 |