Details for New Drug Application (NDA): 211237

NDA 211237 describes ISOPROTERENOL HYDROCHLORIDE, which is a drug marketed by 3M, Alpharma Us Pharms, Abraxis Pharm, Am Regent, Amneal, Amphastar Pharms Inc, Amring Pharms, Avet Lifesciences, Baxter Hlthcare, Cipla, Eugia Pharma, Hikma, Hospira, Intl Medication, Micro Labs, Nexus, Norvium Bioscience, Penn Life, Somerset Theraps Llc, Zydus Pharms, Armour Pharm, DEY, and Parke Davis, and is included in twenty-seven NDAs. It is available from eleven suppliers. Additional details are available on the ISOPROTERENOL HYDROCHLORIDE profile page.

The generic ingredient in ISOPROTERENOL HYDROCHLORIDE is isoproterenol hydrochloride. There are seventeen drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the isoproterenol hydrochloride profile page.

Summary for 211237

Tradename:	ISOPROTERENOL HYDROCHLORIDE
Applicant:	Amring Pharms
Ingredient:	isoproterenol hydrochloride
Patents:	0

Pharmacology for NDA: 211237

Mechanism of Action

Adrenergic beta-Agonists

Suppliers and Packaging for NDA: 211237

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
ISOPROTERENOL HYDROCHLORIDE	isoproterenol hydrochloride	INJECTABLE;INJECTION	211237	ANDA	Nordic Pharma, Inc.	69918-731	69918-731-11	10 VIAL, SINGLE-DOSE in 1 CARTON (69918-731-11) / 1 mL in 1 VIAL, SINGLE-DOSE
ISOPROTERENOL HYDROCHLORIDE	isoproterenol hydrochloride	INJECTABLE;INJECTION	211237	ANDA	Nordic Pharma, Inc.	69918-731	69918-731-10	10 VIAL, SINGLE-DOSE in 1 CARTON (69918-731-10) / 1 mL in 1 VIAL, SINGLE-DOSE

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	INJECTABLE;INJECTION			Strength	0.2MG/ML
Approval Date:	May 19, 2021	TE:	AP	RLD:	No

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