Details for New Drug Application (NDA): 079001
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NDA 079001 describes VECURONIUM BROMIDE, which is a drug marketed by Eugia Pharma, Gland, Hikma, Hospira, Meitheal, Mylan Labs Ltd, Sagent Pharms Inc, Sun Pharm, and Watson Labs, and is included in twelve NDAs. It is available from ten 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. Ten suppliers are listed for this compound. 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. Ten suppliers are listed for this compound. Additional details are available on the vecuronium bromide profile page.
Summary for 079001
| Tradename: | VECURONIUM BROMIDE |
| Applicant: | Sun Pharm |
| Ingredient: | vecuronium bromide |
| Patents: | 0 |
Pharmacology for NDA: 079001
| Physiological Effect | Neuromuscular Nondepolarizing Blockade |
Medical Subject Heading (MeSH) Categories for 079001
Suppliers and Packaging for NDA: 079001
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| VECURONIUM BROMIDE | vecuronium bromide | INJECTABLE;INJECTION | 079001 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-931 | 47335-931-44 | 10 VIAL in 1 BOX (47335-931-44) / 10 mL in 1 VIAL (47335-931-40) |
| VECURONIUM BROMIDE | vecuronium bromide | INJECTABLE;INJECTION | 079001 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-932 | 47335-932-44 | 10 VIAL in 1 BOX (47335-932-44) / 20 mL in 1 VIAL (47335-932-40) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 10MG/VIAL | ||||
| Approval Date: | Jun 17, 2009 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 20MG/VIAL | ||||
| Approval Date: | Jun 17, 2009 | TE: | AP | RLD: | No | ||||
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