Capecitabine 62756-0239
Product NDC
62756-0239- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 1, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA204668
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Capecitabine | 500 mg/1 |
Drug Class
Nucleoside Metabolic Inhibitor [EPC]Nucleic Acid Synthesis Inhibitors [MoA]Nucleoside Metabolic Inhibitor [EPC]
Packaging Options(3)
1000 TABLET, FILM COATED in 1 BOTTLE (62756-239-18)
120 TABLET, FILM COATED in 1 BOTTLE (62756-239-20)
30 TABLET, FILM COATED in 1 BOTTLE (62756-239-83)