doxorubicin hydrochloride
Generic: doxorubicin
Labeler: amneal pharmaceuticals llcDrug Facts
Product Profile
Brand Name
doxorubicin hydrochloride
Generic Name
doxorubicin
Labeler
amneal pharmaceuticals llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
doxorubicin hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70121-1218
Product ID
70121-1218_f4a01f55-65d7-401f-ac2f-e1511bf3a429
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208888
Listing Expiration
2026-12-31
Marketing Start
2017-02-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
701211218
Hyphenated Format
70121-1218
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
doxorubicin hydrochloride (source: ndc)
Generic Name
doxorubicin (source: ndc)
Application Number
ANDA208888 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 10 CARTON in 1 CARTON (70121-1218-7) / 1 VIAL in 1 CARTON (70121-1218-1) / 10 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f4a01f55-65d7-401f-ac2f-e1511bf3a429", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1790095", "1872062"], "spl_set_id": ["d928625e-c1ef-4f25-8d25-764c8c6aab67"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 CARTON (70121-1218-7) / 1 VIAL in 1 CARTON (70121-1218-1) / 10 mL in 1 VIAL", "package_ndc": "70121-1218-7", "marketing_start_date": "20170217"}], "brand_name": "Doxorubicin Hydrochloride", "product_id": "70121-1218_f4a01f55-65d7-401f-ac2f-e1511bf3a429", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "70121-1218", "generic_name": "Doxorubicin", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxorubicin Hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA208888", "marketing_category": "ANDA", "marketing_start_date": "20170217", "listing_expiration_date": "20261231"}