Details for New Drug Application (NDA): 206206
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NDA 206206 describes ROCURONIUM BROMIDE, which is a drug marketed by Caplin, Eugia Pharma, Fresenius Kabi Usa, Gland Pharma Ltd, Hikma, Hospira, Meitheal, Mylan Institutional, Norvium Bioscience, Piramal Critical, Prinston Inc, Sagent Pharms Inc, Sandoz, Shandong, Steriscience, Tamarang, Teva Pharms, and West Ward Pharm Corp, and is included in eighteen NDAs. It is available from twenty-three suppliers. Additional details are available on the ROCURONIUM BROMIDE profile page.
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.
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 206206
| Tradename: | ROCURONIUM BROMIDE |
| Applicant: | Eugia Pharma |
| Ingredient: | rocuronium bromide |
| Patents: | 0 |
Pharmacology for NDA: 206206
| Physiological Effect | Neuromuscular Nondepolarizing Blockade |
Suppliers and Packaging for NDA: 206206
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ROCURONIUM BROMIDE | rocuronium bromide | INJECTABLE;INJECTION | 206206 | ANDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1545 | 51662-1545-1 | 10 mL in 1 VIAL, MULTI-DOSE (51662-1545-1) |
| ROCURONIUM BROMIDE | rocuronium bromide | INJECTABLE;INJECTION | 206206 | ANDA | HF Acquisition Co LLC, DBA HealthFirst | 51662-1546 | 51662-1546-1 | 5 mL in 1 VIAL, MULTI-DOSE (51662-1546-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 50MG/5ML (10MG/ML) | ||||
| Approval Date: | Apr 12, 2017 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 100MG/10ML (10MG/ML) | ||||
| Approval Date: | Apr 12, 2017 | TE: | AP | RLD: | No | ||||
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