beizray

Generic: docetaxel

Labeler: zhuhai beihai biotech co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name beizray
Generic Name docetaxel
Labeler zhuhai beihai biotech co., ltd.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

docetaxel anhydrous 20 mg/mL

Manufacturer
Zhuhai Beihai Biotech Co., Ltd.

Identifiers & Regulatory

Product NDC 83513-008
Product ID 83513-008_45f7d427-0830-1612-e063-6294a90a04d2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA218711
Listing Expiration 2026-12-31
Marketing Start 2025-12-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83513008
Hyphenated Format 83513-008

Supplemental Identifiers

RxCUI
1860480 1860485 2697044 2728902
UPC
0383513009013
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 beizray (source: ndc)
Generic Name docetaxel (source: ndc)
Application Number NDA218711 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (83513-008-01) / 1 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

83513-008-01 1 VIAL, GLASS in 1 CARTON (83513-008-01) / 1 mL in 1 VIAL, GLASS

Ingredients (1)

docetaxel anhydrous (20 mg/mL)

Linked Drug Pages (1)

BEIZRAY ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "45f7d427-0830-1612-e063-6294a90a04d2", "openfda": {"nui": ["N0000175085", "N0000175592"], "upc": ["0383513009013"], "unii": ["699121PHCA"], "rxcui": ["1860480", "1860485", "2697044", "2728902"], "spl_set_id": ["3538b979-8cac-49ed-b8dc-50f73ce38c72"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Zhuhai Beihai Biotech Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (83513-008-01)  / 1 mL in 1 VIAL, GLASS", "package_ndc": "83513-008-01", "marketing_start_date": "20251215"}], "brand_name": "BEIZRAY", "product_id": "83513-008_45f7d427-0830-1612-e063-6294a90a04d2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "83513-008", "generic_name": "Docetaxel", "labeler_name": "Zhuhai Beihai Biotech Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BEIZRAY", "active_ingredients": [{"name": "DOCETAXEL ANHYDROUS", "strength": "20 mg/mL"}], "application_number": "NDA218711", "marketing_category": "NDA", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}