docetaxel

Generic: docetaxel

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name docetaxel
Generic Name docetaxel
Labeler amneal pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

docetaxel anhydrous 20 mg/mL

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 70121-1221
Product ID 70121-1221_350853a3-6178-4d83-b5c4-75b3e4c1799d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209640
Listing Expiration 2026-12-31
Marketing Start 2018-01-19

Pharmacologic Class

Established (EPC)
microtubule inhibitor [epc]
Physiologic Effect
microtubule inhibition [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 701211221
Hyphenated Format 70121-1221

Supplemental Identifiers

RxCUI
1860480 1860485 1861411
UPC
0370121122111 0370121122210 0370121122319
UNII
699121PHCA
NUI
N0000175085 N0000175592

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 docetaxel (source: ndc)
Generic Name docetaxel (source: ndc)
Application Number ANDA209640 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (70121-1221-1) / 1 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (1)

docetaxel anhydrous (20 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "350853a3-6178-4d83-b5c4-75b3e4c1799d", "openfda": {"nui": ["N0000175085", "N0000175592"], "upc": ["0370121122111", "0370121122210", "0370121122319"], "unii": ["699121PHCA"], "rxcui": ["1860480", "1860485", "1861411"], "spl_set_id": ["67508df6-b96f-46fa-a792-0afcdfa9810e"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (70121-1221-1)  / 1 mL in 1 VIAL, GLASS", "package_ndc": "70121-1221-1", "marketing_start_date": "20180119"}], "brand_name": "Docetaxel", "product_id": "70121-1221_350853a3-6178-4d83-b5c4-75b3e4c1799d", "dosage_form": "INJECTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "70121-1221", "generic_name": "Docetaxel", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL ANHYDROUS", "strength": "20 mg/mL"}], "application_number": "ANDA209640", "marketing_category": "ANDA", "marketing_start_date": "20180119", "listing_expiration_date": "20261231"}