Details for New Drug Application (NDA): 214529
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The generic ingredient in CYCLOPHOSPHAMIDE 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 214529
Tradename: | CYCLOPHOSPHAMIDE |
Applicant: | Sagent Pharms Inc |
Ingredient: | cyclophosphamide |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 214529
Suppliers and Packaging for NDA: 214529
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CYCLOPHOSPHAMIDE | cyclophosphamide | INJECTABLE;INJECTION | 214529 | ANDA | Sagent Pharmaceuticals | 25021-247 | 25021-247-50 | 1 VIAL in 1 CARTON (25021-247-50) / 25 mL in 1 VIAL |
CYCLOPHOSPHAMIDE | cyclophosphamide | INJECTABLE;INJECTION | 214529 | ANDA | Sagent Pharmaceuticals | 25021-248 | 25021-248-51 | 1 VIAL in 1 CARTON (25021-248-51) / 50 mL in 1 VIAL |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 500MG/VIAL | ||||
Approval Date: | Jul 17, 2023 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 1GM/VIAL | ||||
Approval Date: | Jul 17, 2023 | TE: | AP | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2GM/VIAL | ||||
Approval Date: | Jul 17, 2023 | TE: | AP | RLD: | No |
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