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Last Updated: April 20, 2024

Details for New Drug Application (NDA): 212015


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NDA 212015 describes ERYTHROMYCIN, which is a drug marketed by Arbor Pharms Llc, Barr, Encube, Fougera Pharms, Padagis Us, Elkins Sinn, Bausch And Lomb, Pharmaderm, Pharmafair, Sentiss, Paddock Llc, Alpharma Us Pharms, Bausch, Lilly, Pai Holdings Pharm, Pharmobedient Cnsltg, Renaissance Pharma, Epic Pharma Llc, Mylan, Amneal Pharms Co, Torrent, Alembic, Alkem Labs Ltd, Cadila Pharms Ltd, Teva Pharms Usa Inc, Zydus, Zydus Pharms, Lyne, Ivax Sub Teva Pharms, Watson Labs, Cosette, Life Labs, Amneal Pharms, Ani Pharms, Par Pharm Inc, Dista, Naska, Parke Davis, Aurobindo Pharma Usa, Abraxis Pharm, Baxter Hlthcare, Exela Pharma, Nexus, Teva Parenteral, Lederle, and Purepac Pharm, and is included in seventy-six NDAs. It is available from thirty suppliers. Additional details are available on the ERYTHROMYCIN profile page.

The generic ingredient in ERYTHROMYCIN is erythromycin stearate. There are one hundred and three drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the erythromycin stearate profile page.
Summary for 212015
Tradename:ERYTHROMYCIN
Applicant:Torrent
Ingredient:erythromycin
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 212015
Medical Subject Heading (MeSH) Categories for 212015
Suppliers and Packaging for NDA: 212015
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
ERYTHROMYCIN erythromycin TABLET;ORAL 212015 ANDA Torrent Pharmaceuticals Limited 13668-606 13668-606-01 100 TABLET, COATED in 1 BOTTLE (13668-606-01)
ERYTHROMYCIN erythromycin TABLET;ORAL 212015 ANDA Torrent Pharmaceuticals Limited 13668-606 13668-606-05 500 TABLET, COATED in 1 BOTTLE (13668-606-05)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength250MG
Approval Date:Jul 6, 2020TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength500MG
Approval Date:Jul 6, 2020TE:ABRLD:No

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