Package 47335-323-40

Brand: docetaxel

Generic: docetaxel
NDC Package

Package Facts

Identity

Package NDC 47335-323-40
Digits Only 4733532340
Product NDC 47335-323
Product ID 47335-323_9a0d7b91-4324-4e19-9cd8-eb19266e771a
Description

1 VIAL, GLASS in 1 CARTON (47335-323-40) / 1 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2020-11-26
Brand docetaxel
Generic docetaxel
Sample Package No

Linked Drug Pages (1)

Docetaxel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "9a0d7b91-4324-4e19-9cd8-eb19266e771a", "openfda": {"nui": ["N0000175085", "N0000175592"], "unii": ["699121PHCA"], "rxcui": ["1860480", "1860485", "1861411"], "spl_set_id": ["c85b2c62-3c33-4cbc-8b79-d5e17851a1b4"], "pharm_class_pe": ["Microtubule Inhibition [PE]"], "pharm_class_epc": ["Microtubule Inhibitor [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (47335-323-40)  / 1 mL in 1 VIAL, GLASS", "package_ndc": "47335-323-40", "marketing_start_date": "20201126"}], "brand_name": "Docetaxel", "product_id": "47335-323_9a0d7b91-4324-4e19-9cd8-eb19266e771a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "47335-323", "generic_name": "Docetaxel", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL ANHYDROUS", "strength": "20 mg/mL"}], "application_number": "NDA022534", "marketing_category": "NDA", "marketing_start_date": "20201126", "listing_expiration_date": "20261231"}