NDC 62756-239 – Capecitabine
Capecitabine 500 mg/1 · Tablet, Film Coated · Oral
Product NDC62756-239
Product details
- Brand name
- Capecitabine
- Generic name
- Capecitabine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204668
- Marketed since
- September 1, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nucleoside Metabolic Inhibitor
Active ingredients
- Capecitabine 500 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 62756-239-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (62756-239-18) | Sep 1, 2019 |
| 62756-239-20 | 120 TABLET, FILM COATED in 1 BOTTLE (62756-239-20) | Sep 1, 2019 |
| 62756-239-83 | 30 TABLET, FILM COATED in 1 BOTTLE (62756-239-83) | Sep 1, 2019 |
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