doxorubicin hydrochloride
Generic: doxorubicin hydrochloride
Labeler: alembic pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
doxorubicin hydrochloride
Generic Name
doxorubicin hydrochloride
Labeler
alembic pharmaceuticals limited
Dosage Form
INJECTION, SUSPENSION, LIPOSOMAL
Routes
Active Ingredients
doxorubicin hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
46708-810
Product ID
46708-810_f8e001f5-441c-47cd-86f6-5d5e3de16bc0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA219199
Listing Expiration
2026-12-31
Marketing Start
2025-06-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
46708810
Hyphenated Format
46708-810
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 hydrochloride (source: ndc)
Application Number
ANDA219199 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (46708-810-10) / 10 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": "f8e001f5-441c-47cd-86f6-5d5e3de16bc0", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1790115", "1790127"], "spl_set_id": ["f8e001f5-441c-47cd-86f6-5d5e3de16bc0"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (46708-810-10) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "46708-810-10", "marketing_start_date": "20250627"}], "brand_name": "doxorubicin hydrochloride", "product_id": "46708-810_f8e001f5-441c-47cd-86f6-5d5e3de16bc0", "dosage_form": "INJECTION, SUSPENSION, LIPOSOMAL", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "46708-810", "generic_name": "doxorubicin hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxorubicin hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA219199", "marketing_category": "ANDA", "marketing_start_date": "20250627", "listing_expiration_date": "20261231"}