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Last Updated: November 25, 2024

Details for New Drug Application (NDA): 217685


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NDA 217685 describes DOXYCYCLINE HYCLATE, which is a drug marketed by Pliva, Bausch, Actavis Labs Fl Inc, Ajanta Pharma Ltd, Alembic, Amneal Pharms, Changzhou Pharm, Chartwell, Halsey, Heather, Hikma Intl Pharms, Interpharm, Mutual Pharm, Nesher Pharms, Nostrum Labs Inc, Par Pharm, Pvt Form, Ranbaxy, Strides Pharma, Sun Pharm Industries, Superpharm, Warner Chilcott, Watson Labs, Zhejiang Yongtai, Zydus Lifesciences, Endo Operations, Gland Pharma Ltd, Heritage, Lupin Ltd, Slate Run Pharma, West-ward Pharms Int, Actavis Elizabeth, Aurobindo Pharma Usa, Impax Labs Inc, Lupin, Prinston Inc, Rising, Zydus Pharms, Acella, Amneal, Amneal Pharms Co, Apotex, Avet Lifesciences, Caribe Holdings, Chartwell Molecular, Dr Reddys Labs Sa, Epic Pharma Llc, Heritage Pharma, Larken Labs, Mylan, Novel Labs Inc, Oryza, Praxgen, and Torrent, and is included in eighty-one NDAs. It is available from sixty-five suppliers. Additional details are available on the DOXYCYCLINE HYCLATE profile page.

The generic ingredient in DOXYCYCLINE HYCLATE is doxycycline hyclate. There are twenty-eight drug master file entries for this compound. Seventy-four suppliers are listed for this compound. Additional details are available on the doxycycline hyclate profile page.
Summary for 217685
Tradename:DOXYCYCLINE HYCLATE
Applicant:Slate Run Pharma
Ingredient:doxycycline hyclate
Patents:0
Pharmacology for NDA: 217685
Suppliers and Packaging for NDA: 217685
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DOXYCYCLINE HYCLATE doxycycline hyclate INJECTABLE;INJECTION 217685 ANDA Slate Run Pharmaceuticals, LLC 70436-032 70436-032-82 10 VIAL, SINGLE-DOSE in 1 CARTON (70436-032-82) / 10 mL in 1 VIAL, SINGLE-DOSE (70436-032-35)
DOXYCYCLINE HYCLATE doxycycline hyclate INJECTABLE;INJECTION 217685 ANDA Slate Run Pharmaceuticals, LLC 70436-201 70436-201-82 10 VIAL, SINGLE-DOSE in 1 CARTON (70436-201-82) / 20 mL in 1 VIAL, SINGLE-DOSE (70436-201-36)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 100MG BASE/VIAL
Approval Date:Jun 21, 2024TE:APRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 200MG BASE/VIAL
Approval Date:Jun 21, 2024TE:APRLD:No

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