docetaxel

Generic: docetaxel

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name docetaxel
Generic Name docetaxel
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

docetaxel 20 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-903
Product ID 23155-903_c2351485-3f3d-40fb-8fd6-f45c01d66394
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216677
Listing Expiration 2026-12-31
Marketing Start 2024-12-15

Pharmacologic Class

Classes
microtubule inhibition [pe] microtubule inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155903
Hyphenated Format 23155-903

Supplemental Identifiers

RxCUI
1860480 1860485 1861411
UPC
0323155903317 0323155905311
UNII
15H5577CQD

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 ANDA216677 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 INJECTION in 1 CARTON (23155-903-31)
source: ndc

Packages (1)

Ingredients (1)

docetaxel (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c2351485-3f3d-40fb-8fd6-f45c01d66394", "openfda": {"upc": ["0323155903317", "0323155905311"], "unii": ["15H5577CQD"], "rxcui": ["1860480", "1860485", "1861411"], "spl_set_id": ["81686d37-a13f-46e2-b439-a84eb1433634"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION in 1 CARTON (23155-903-31)", "package_ndc": "23155-903-31", "marketing_start_date": "20241215"}], "brand_name": "Docetaxel", "product_id": "23155-903_c2351485-3f3d-40fb-8fd6-f45c01d66394", "dosage_form": "INJECTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "23155-903", "generic_name": "Docetaxel", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/1"}], "application_number": "ANDA216677", "marketing_category": "ANDA", "marketing_start_date": "20241215", "listing_expiration_date": "20261231"}