cyclophosphamide

Generic: cyclophosphamide

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclophosphamide
Generic Name cyclophosphamide
Labeler northstar rx llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS ORAL
Active Ingredients

cyclophosphamide 1 g/50mL

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 16714-857
Product ID 16714-857_27e82150-4ad3-5be6-e063-6394a90a0e3f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204555
Listing Expiration 2026-12-31
Marketing Start 2019-01-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714857
Hyphenated Format 16714-857

Supplemental Identifiers

RxCUI
1734917 1734919 1734921
UNII
8N3DW7272P

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cyclophosphamide (source: ndc)
Generic Name cyclophosphamide (source: ndc)
Application Number ANDA204555 (source: ndc)
Routes
INTRAVENOUS ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/50mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (16714-857-01) / 50 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

cyclophosphamide (1 g/50mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "ORAL"], "spl_id": "27e82150-4ad3-5be6-e063-6394a90a0e3f", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["76f057be-e3da-0a89-e053-2a91aa0a8438"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (16714-857-01)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "16714-857-01", "marketing_start_date": "20190108"}], "brand_name": "Cyclophosphamide", "product_id": "16714-857_27e82150-4ad3-5be6-e063-6394a90a0e3f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "16714-857", "generic_name": "cyclophosphamide", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "1 g/50mL"}], "application_number": "ANDA204555", "marketing_category": "ANDA", "marketing_start_date": "20190108", "listing_expiration_date": "20261231"}