Details for New Drug Application (NDA): 074688
NDA 074688 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 is one drug master file entry 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 is one drug master file entry for this compound. Ten suppliers are listed for this compound. Additional details are available on the vecuronium bromide profile page.
Summary for 074688
| Tradename: | VECURONIUM BROMIDE |
| Applicant: | Meitheal |
| Ingredient: | vecuronium bromide |
| Patents: | 0 |
Pharmacology for NDA: 074688
| Physiological Effect | Neuromuscular Nondepolarizing Blockade |
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 | Meitheal Pharmaceuticals Inc. | 71288-744 | 71288-744-11 | 10 VIAL, SINGLE-USE in 1 CARTON (71288-744-11) / 10 mL in 1 VIAL, SINGLE-USE (71288-744-10) |
| VECURONIUM BROMIDE | vecuronium bromide | INJECTABLE;INJECTION | 074688 | ANDA | Meitheal Pharmaceuticals Inc. | 71288-745 | 71288-745-21 | 10 VIAL, SINGLE-USE in 1 CARTON (71288-745-21) / 20 mL in 1 VIAL, SINGLE-USE (71288-745-20) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 10MG/VIAL | ||||
| Approval Date: | Aug 25, 1999 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 20MG/VIAL | ||||
| Approval Date: | Aug 25, 1999 | TE: | AP | RLD: | No | ||||
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