Details for New Drug Application (NDA): 211005

NDA 211005 describes HEPARIN SODIUM, which is a drug marketed by Abraxis Pharm, Aspen Global Inc, B Braun Medical Inc, Be Pharms, Casi Pharms Inc, Chamberlin Parenterl, Dell Labs, Dr Reddys, Epic Pharma Llc, Fresenius Kabi Usa, Gland, Hikma, Hospira, Hospira Inc, Lilly, Luitpold, Mylan Labs Ltd, Nanjing King-friend, Parke Davis, Pfizer, Pharm Spec, Pharmacia And Upjohn, Sagent Pharms, Sandoz, Shenzhen Techdow, Smith And Nephew, Solopak, Watson Labs Inc, Baxter Hlthcare, Mcgaw, B Braun, and Pharma Serve Ny, and is included in sixty-nine NDAs. It is available from twenty suppliers. Additional details are available on the HEPARIN SODIUM profile page.

The generic ingredient in HEPARIN SODIUM is heparin sodium. There are seventy-seven drug master file entries for this compound. Twenty-two suppliers are listed for this compound. Additional details are available on the heparin sodium profile page.

Summary for 211005

Tradename:	HEPARIN SODIUM
Applicant:	Nanjing King-friend
Ingredient:	heparin sodium
Patents:	0

Pharmacology for NDA: 211005

Suppliers and Packaging for NDA: 211005

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
HEPARIN SODIUM	heparin sodium	INJECTABLE;INJECTION	211005	ANDA	Meitheal Pharmaceuticals Inc.	71288-400	71288-400-03	25 VIAL, SINGLE-DOSE in 1 CARTON (71288-400-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-400-02)
HEPARIN SODIUM	heparin sodium	INJECTABLE;INJECTION	211005	ANDA	NorthStar RxLLC	72603-336	72603-336-25	25 VIAL, SINGLE-DOSE in 1 CARTON (72603-336-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72603-336-01)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	INJECTABLE;INJECTION			Strength	1,000 UNITS/ML
Approval Date:	Dec 14, 2018	TE:	AP	RLD:	No

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