NDC 0480-4053 – Gefitinib
Gefitinib 250 mg/1 · Tablet, Film Coated · Oral
Product NDC0480-4053
Product details
- Brand name
- Gefitinib
- Generic name
- Gefitinib
- Labeler
- Teva Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208913
- Marketed since
- June 21, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Kinase Inhibitor
Active ingredients
- Gefitinib 250 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0480-4053-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0480-4053-56) | Jun 21, 2023 |
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