CYCLOPHOSPHAMIDE

Product NDC

10019-990

11-digit product format

100190990

Labeler code

10019

Product ID

10019-990_3082cff4-7019-42cf-ae82-ac5af74af797

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclophosphamide

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS; ORAL

Labeler

Baxter Healthcare Corporation

Application

NDA012142

Marketing category

NDA

Marketing start

1959-11-16

Marketing end

0000-00-00

Substance

CYCLOPHOSPHAMIDE

Active strength

2 g/100mL

Pharmacologic classes

Alkylating Activity [MoA],Alkylating Drug [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record