NDC 67877-225 – Mycophenolate Mofetil
Mycophenolate Mofetil 500 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-225
Product details
- Brand name
- Mycophenolate Mofetil
- Generic name
- Mycophenolate Mofetil
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091249
- Marketed since
- November 28, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antimetabolite Immunosuppressant
Active ingredients
- Mycophenolate Mofetil 500 mg/1
Uses, dosage, side effects and warnings for Mycophenolate Mofetil →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-225-01 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-225-01) | Nov 28, 2011 |
| 67877-225-05 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-225-05) | Nov 28, 2011 |
| 67877-225-38 | 10 BLISTER PACK in 1 CARTON (67877-225-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Nov 28, 2011 |
| 67877-225-84 | 3 BLISTER PACK in 1 CARTON (67877-225-84) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Nov 28, 2011 |
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