Details for New Drug Application (NDA): 210203
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The generic ingredient in CAPECITABINE is capecitabine. There are twenty-eight drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the capecitabine profile page.
Summary for 210203
Tradename: | CAPECITABINE |
Applicant: | Hetero Labs Ltd V |
Ingredient: | capecitabine |
Patents: | 0 |
Pharmacology for NDA: 210203
Mechanism of Action | Nucleic Acid Synthesis Inhibitors |
Medical Subject Heading (MeSH) Categories for 210203
Suppliers and Packaging for NDA: 210203
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CAPECITABINE | capecitabine | TABLET;ORAL | 210203 | ANDA | Camber Pharmaceuticals, Inc. | 31722-774 | 31722-774-60 | 60 TABLET, FILM COATED in 1 BOTTLE (31722-774-60) |
CAPECITABINE | capecitabine | TABLET;ORAL | 210203 | ANDA | Camber Pharmaceuticals, Inc. | 31722-775 | 31722-775-12 | 120 TABLET, FILM COATED in 1 BOTTLE (31722-775-12) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 150MG | ||||
Approval Date: | Mar 5, 2024 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 500MG | ||||
Approval Date: | Mar 5, 2024 | TE: | AB | RLD: | No |
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