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Last Updated: August 11, 2020

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Details for New Drug Application (NDA): 074688

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NDA 074688 describes VECURONIUM BROMIDE, which is a drug marketed by Aurobindo Pharma Ltd, Gland Pharma Ltd, Hikma, Hospira, Mylan Labs Ltd, Sagent Pharms Inc, Sun Pharm, Teva Pharms Usa, Watson Labs, and West-ward Pharms Int, and is included in twelve NDAs. It is available from nine suppliers. Additional details are available on the VECURONIUM BROMIDE profile page.

The generic ingredient in VECURONIUM BROMIDE is vecuronium bromide. There are six drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the vecuronium bromide profile page.
Summary for 074688
Tradename:VECURONIUM BROMIDE
Applicant:Teva Pharms Usa
Ingredient:vecuronium bromide
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 074688
Medical Subject Heading (MeSH) Categories for 074688
Suppliers and Packaging for NDA: 074688
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
VECURONIUM BROMIDE vecuronium bromide INJECTABLE;INJECTION 074688 ANDA Teva Parenteral Medicines, Inc. 0703-2914 0703-2914-03 10 VIAL, SINGLE-USE in 1 CARTON (0703-2914-03) > 10 mL in 1 VIAL, SINGLE-USE (0703-2914-01)
VECURONIUM BROMIDE vecuronium bromide INJECTABLE;INJECTION 074688 ANDA Teva Parenteral Medicines, Inc. 0703-2925 0703-2925-03 10 VIAL, SINGLE-USE in 1 CARTON (0703-2925-03) > 20 mL in 1 VIAL, SINGLE-USE (0703-2925-01)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength10MG/VIAL
Approval Date:Aug 25, 1999TE:APRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength20MG/VIAL
Approval Date:Aug 25, 1999TE:APRLD:No

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