NDC 70771-1058 – Methotrexate
Methotrexate 2.5 mg/1 · Tablet · Oral
Product NDC70771-1058
Product details
- Brand name
- Methotrexate
- Generic name
- Methotrexate
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207812
- Marketed since
- February 9, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Folate Analog Metabolic Inhibitor
Active ingredients
- Methotrexate 2.5 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1058-0 | 1000 TABLET in 1 BOTTLE (70771-1058-0) | Feb 9, 2017 |
| 70771-1058-1 | 100 TABLET in 1 BOTTLE (70771-1058-1) | Feb 9, 2017 |
| 70771-1058-3 | 36 TABLET in 1 BOTTLE (70771-1058-3) | Feb 9, 2017 |
| 70771-1058-5 | 500 TABLET in 1 BOTTLE (70771-1058-5) | Feb 9, 2017 |
| 70771-1058-7 | 100 BLISTER PACK in 1 CARTON (70771-1058-7) / 1 TABLET in 1 BLISTER PACK (70771-1058-2) | Feb 9, 2017 |
| 70771-1058-9 | 90 TABLET in 1 BOTTLE (70771-1058-9) | Feb 9, 2017 |
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