NDC 23155-836 – Mycophenolate mofetil
Mycophenolate Mofetil 500 mg/1 · Tablet, Film Coated · Oral
Product NDC23155-836
Product details
- Brand name
- Mycophenolate mofetil
- Generic name
- Mycophenolate mofetil
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090456
- Marketed since
- October 15, 2022
- Marketing end
- May 31, 2028
- Pharmacologic class
- Antimetabolite Immunosuppressant
Active ingredients
- Mycophenolate Mofetil 500 mg/1
Uses, dosage, side effects and warnings for Mycophenolate Mofetil →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 23155-836-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (23155-836-01) | Oct 15, 2022 |
| 23155-836-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (23155-836-05) | Oct 15, 2022 |
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