24979-715 : Sorafenib 200 mg Oral Tablet, Film Coated
NDC: | 24979-715 |
Labeler: | Twi Pharmaceuticals USA, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Sorafenib |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA209050 |
Rev. Date: |
NDC Package Codes:
- 24979-715-04: 60 TABLET, FILM COATED IN 1 BOTTLE (24979‑715‑04)
- 24979-715-44: 120 TABLET, FILM COATED IN 1 BOTTLE (24979‑715‑44)
Active Ingredients:
- Sorafenib
Dosage Strength:
- 200 mg
Pharmaceutical Classes:
- Kinase Inhibitor [EPC]
- Protein Kinase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 0480-5425 Sorafenib 200 mg Oral Tablet, Film Coated by Teva Pharmaceuticals, Inc.
- 13668-682 Sorafenib 200 mg Oral Tablet, Film Coated by Torrent Pharmaceuticals Limited
- 43598-458 Sorafenib 200 mg Oral Tablet, Film Coated by Dr.reddys Laboratories Inc
- 43826-066 Sorafenib 200 mg Oral Tablet, Film Coated by Bora Pharmaceutical Laboratories Inc.
- 51407-760 Sorafenib 200 mg Oral Tablet, Film Coated by Golden State Medical Supply, Inc.
- 51990-201 Sorafenib 200 mg Oral Tablet, Film Coated by Yabao Pharmaceutical Co., Ltd. Beijing
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.