doxorubicin hydrochloride
Generic: doxorubicin hydrochloride
Labeler: northstar rxllcDrug Facts
Product Profile
Brand Name
doxorubicin hydrochloride
Generic Name
doxorubicin hydrochloride
Labeler
northstar rxllc
Dosage Form
INJECTABLE, LIPOSOMAL
Routes
Active Ingredients
doxorubicin hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
16714-856
Product ID
16714-856_515391d8-92bc-84e3-2408-79a2d0b35ed2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208657
Listing Expiration
2026-12-31
Marketing Start
2017-08-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714856
Hyphenated Format
16714-856
Supplemental Identifiers
RxCUI
UPC
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 hydrochloride (source: ndc)
Application Number
ANDA208657 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (16714-856-01) / 25 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "515391d8-92bc-84e3-2408-79a2d0b35ed2", "openfda": {"upc": ["0316714742014"], "unii": ["82F2G7BL4E"], "rxcui": ["1790115", "1790127"], "spl_set_id": ["67417a18-e0f4-c9a0-e152-b8d8dc934af6"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (16714-856-01) / 25 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "16714-856-01", "marketing_start_date": "20170829"}], "brand_name": "Doxorubicin Hydrochloride", "product_id": "16714-856_515391d8-92bc-84e3-2408-79a2d0b35ed2", "dosage_form": "INJECTABLE, LIPOSOMAL", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "16714-856", "generic_name": "Doxorubicin Hydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxorubicin Hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA208657", "marketing_category": "ANDA", "marketing_start_date": "20170829", "listing_expiration_date": "20261231"}