NDC 71288-143

Docetaxel anhydrous

Docetaxel Anhydrous

Docetaxel anhydrous is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Meitheal Pharmaceuticals Inc. The primary component is Docetaxel Anhydrous.

Product ID71288-143_bde535be-817f-4e14-e053-2a95a90a7b4f
NDC71288-143
Product TypeHuman Prescription Drug
Proprietary NameDocetaxel anhydrous
Generic NameDocetaxel Anhydrous
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2018-08-24
Marketing CategoryANDA / ANDA
Application NumberANDA209634
Labeler NameMeitheal Pharmaceuticals Inc
Substance NameDOCETAXEL ANHYDROUS
Active Ingredient Strength20 mg/2mL
Pharm ClassesMicrotubule Inhibition [PE],Microtubule Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 71288-143-02

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-143-02) > 2 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date2018-08-24
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Docetaxel anhydrous" or generic name "Docetaxel Anhydrous"

NDCBrand NameGeneric Name
69097-369Docetaxel AnhydrousDocetaxel Anhydrous
69097-371Docetaxel AnhydrousDocetaxel Anhydrous
69097-372Docetaxel AnhydrousDocetaxel Anhydrous
71288-144Docetaxel anhydrousDocetaxel anhydrous
71288-143Docetaxel anhydrousDocetaxel anhydrous
0409-0016DocetaxelDOCETAXEL ANHYDROUS
0409-0201DocetaxelDOCETAXEL ANHYDROUS
0409-1732DocetaxelDOCETAXEL ANHYDROUS
0409-2026DocetaxelDOCETAXEL ANHYDROUS
0409-7870DocetaxelDOCETAXEL ANHYDROUS
25021-245DocetaxelDocetaxel Anhydrous
50742-428DOCETAXELDOCETAXEL ANHYDROUS
50742-431DOCETAXELDOCETAXEL ANHYDROUS
50742-463DOCETAXELDOCETAXEL ANHYDROUS
67457-531DocetaxelDOCETAXEL ANHYDROUS
67457-532DocetaxelDOCETAXEL ANHYDROUS
67457-533DocetaxelDOCETAXEL ANHYDROUS

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