NDC 60687-438 – Mycophenolate mofetil
Mycophenolate Mofetil 500 mg/1 · Tablet, Film Coated · Oral
Product NDC60687-438
Product details
- Brand name
- Mycophenolate mofetil
- Generic name
- Mycophenolate Mofetil
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090456
- Marketed since
- June 14, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antimetabolite Immunosuppressant
Active ingredients
- Mycophenolate Mofetil 500 mg/1
Uses, dosage, side effects and warnings for Mycophenolate Mofetil →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 60687-438-01 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-438-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-438-11) | Jun 14, 2019 |
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