Details for New Drug Application (NDA): 212668
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The generic ingredient in ROCURONIUM BROMIDE is rocuronium bromide. There are eleven drug master file entries for this compound. Twenty-three suppliers are listed for this compound. Additional details are available on the rocuronium bromide profile page.
Summary for 212668
Tradename: | ROCURONIUM BROMIDE |
Applicant: | Prinston Inc |
Ingredient: | rocuronium bromide |
Patents: | 0 |
Pharmacology for NDA: 212668
Physiological Effect | Neuromuscular Nondepolarizing Blockade |
Suppliers and Packaging for NDA: 212668
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ROCURONIUM BROMIDE | rocuronium bromide | INJECTABLE;INJECTION | 212668 | ANDA | Solco Healthcare US, LLC | 43547-530 | 43547-530-10 | 10 VIAL, MULTI-DOSE in 1 CARTON (43547-530-10) / 5 mL in 1 VIAL, MULTI-DOSE (43547-530-01) |
ROCURONIUM BROMIDE | rocuronium bromide | INJECTABLE;INJECTION | 212668 | ANDA | Solco Healthcare US, LLC | 43547-531 | 43547-531-10 | 10 VIAL, MULTI-DOSE in 1 CARTON (43547-531-10) / 10 mL in 1 VIAL, MULTI-DOSE (43547-531-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 50MG/5ML (10MG/ML) | ||||
Approval Date: | May 26, 2022 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 100MG/10ML (10MG/ML) | ||||
Approval Date: | May 26, 2022 | TE: | AP | RLD: | No |
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