Details for New Drug Application (NDA): 012141
✉ Email this page to a colleague
The generic ingredient in CYTOXAN is cyclophosphamide. There are nineteen drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the cyclophosphamide profile page.
Summary for 012141
Tradename: | CYTOXAN |
Applicant: | Baxter Hlthcare |
Ingredient: | cyclophosphamide |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 012141
Suppliers and Packaging for NDA: 012141
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CYTOXAN | cyclophosphamide | TABLET;ORAL | 012141 | NDA AUTHORIZED GENERIC | Baxter Healthcare Corporation | 10019-982 | 10019-982-01 | 1 BOTTLE in 1 CARTON (10019-982-01) / 100 TABLET in 1 BOTTLE (10019-982-09) |
CYTOXAN | cyclophosphamide | TABLET;ORAL | 012141 | NDA | Baxter Healthcare Corporation | 10019-984 | 10019-984-01 | 1 BOTTLE in 1 CARTON (10019-984-01) / 100 TABLET in 1 BOTTLE (10019-984-09) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes |
Complete Access Available with Subscription