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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 209045


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NDA 209045 describes AZITHROMYCIN, which is a drug marketed by Amneal, Aurobindo Pharma Ltd, Chartwell Rx, Epic Pharma Llc, Hainan Poly, Pliva, Sandoz, Taro, Teva Pharms, Zydus Lifesciences, Eugia Pharma, Fresenius Kabi Usa, Gland Pharma Ltd, Hikma, Hospira, Norvium Bioscience, Rising, Slate Run Pharma, Sun Pharm Inds Ltd, Teva Parenteral, Alembic, Apotex Corp, Aurobindo Pharma Usa, Bionpharma, Cspc Ouyi, Lupin Ltd, Pharmobedient, Strides Pharma, Sunshine, Teva, Yung Shin Pharm, and Zydus Pharms, and is included in sixty-three NDAs. It is available from sixty-two suppliers. Additional details are available on the AZITHROMYCIN profile page.

The generic ingredient in AZITHROMYCIN is azithromycin. There are thirty-two drug master file entries for this compound. Sixty-seven suppliers are listed for this compound. Additional details are available on the azithromycin profile page.
Summary for 209045
Tradename:AZITHROMYCIN
Applicant:Sunshine
Ingredient:azithromycin
Patents:0
Pharmacology for NDA: 209045
Medical Subject Heading (MeSH) Categories for 209045
Suppliers and Packaging for NDA: 209045
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
AZITHROMYCIN azithromycin TABLET;ORAL 209045 ANDA Lannett Company, Inc. 0527-2370 0527-2370-20 6 TABLET, FILM COATED in 1 BLISTER PACK (0527-2370-20)
AZITHROMYCIN azithromycin TABLET;ORAL 209045 ANDA Lannett Company, Inc. 0527-2370 0527-2370-32 30 TABLET, FILM COATED in 1 BOTTLE (0527-2370-32)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrengthEQ 250MG BASE
Approval Date:Dec 7, 2018TE:ABRLD:No

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