Details for New Drug Application (NDA): 075164
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The generic ingredient in VECURONIUM BROMIDE is vecuronium bromide. There are six drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the vecuronium bromide profile page.
Summary for 075164
Tradename: | VECURONIUM BROMIDE |
Applicant: | Hospira |
Ingredient: | vecuronium bromide |
Patents: | 0 |
Pharmacology for NDA: 075164
Physiological Effect | Neuromuscular Nondepolarizing Blockade |
Medical Subject Heading (MeSH) Categories for 075164
Suppliers and Packaging for NDA: 075164
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
VECURONIUM BROMIDE | vecuronium bromide | INJECTABLE;INJECTION | 075164 | ANDA | Hospira, Inc. | 0409-1632 | 0409-1632-01 | 10 VIAL in 1 CARTON (0409-1632-01) / 10 mL in 1 VIAL (0409-1632-21) |
VECURONIUM BROMIDE | vecuronium bromide | INJECTABLE;INJECTION | 075164 | ANDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1475 | 51662-1475-1 | 10 mL in 1 VIAL (51662-1475-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 10MG/VIAL | ||||
Approval Date: | Oct 21, 1999 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 20MG/VIAL | ||||
Approval Date: | Oct 21, 1999 | TE: | AP | RLD: | No |
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