DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 090809
describes HEPARIN SODIUM
, which is a drug marketed by Hospira, Sandoz, Eurohlth Intl Sarl, Solopak, Watson Labs Inc, Sagent Pharms, Lilly, Gland Pharma Ltd, Fresenius Kabi Usa, Chamberlin Parenterl, Abraxis Pharm, Shenzhen Techdow, West-ward Pharms Int, Smith And Nephew, Dell Labs, Parke Davis, Luitpold, Organon Usa Inc, Watson Labs, Pfizer, Pharmacia And Upjohn, Hospira Inc, Pharm Spec, Akorn, Baxter Hlthcare, Mcgaw, B Braun, and Pharma Serve Ny, and is included in fifty-eight NDAs. It is available from twelve suppliers. Additional details are available on the HEPARIN SODIUM profile page.
The generic ingredient in HEPARIN SODIUM is heparin sodium. There are seventy-six drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the heparin sodium profile page.
Summary for NDA: 090809
|Formulation / Manufacturing:||see details|
Pharmacology for NDA: 090809
Suppliers and Packaging for NDA: 090809
||National Drug Code
||25 VIAL in 1 CARTON (25021-404-01) > 1 mL in 1 VIAL
|Complete Access Available with Subscription
Summary for product number 001
|Active Rx/OTC/Discontinued:||RX||Dosage:||INJECTABLE;INJECTION||Strength||20,000 UNITS/ML|
|Approval Date:||Jun 30, 2010||TE:||AP||RLD:||No|
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