Details for New Drug Application (NDA): 020551
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NDA 020551 describes NIMBEX PRESERVATIVE FREE, which is a drug marketed by Abbvie and is included in one NDA. It is available from one supplier. Additional details are available on the NIMBEX PRESERVATIVE FREE profile page.
The generic ingredient in NIMBEX PRESERVATIVE FREE is cisatracurium besylate. There are nine drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the cisatracurium besylate profile page.
The generic ingredient in NIMBEX PRESERVATIVE FREE is cisatracurium besylate. There are nine drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the cisatracurium besylate profile page.
Summary for 020551
| Tradename: | NIMBEX PRESERVATIVE FREE |
| Applicant: | Abbvie |
| Ingredient: | cisatracurium besylate |
| Patents: | 0 |
Pharmacology for NDA: 020551
| Physiological Effect | Neuromuscular Nondepolarizing Blockade |
Suppliers and Packaging for NDA: 020551
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| NIMBEX | cisatracurium besylate | INJECTABLE;INJECTION | 020551 | NDA | AbbVie Inc. | 0074-4378 | 0074-4378-05 | 5 mL in 1 VIAL, SINGLE-DOSE (0074-4378-05) |
| NIMBEX | cisatracurium besylate | INJECTABLE;INJECTION | 020551 | NDA | AbbVie Inc. | 0074-4380 | 0074-4380-10 | 10 mL in 1 VIAL, MULTI-DOSE (0074-4380-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 2MG BASE/ML | ||||
| Approval Date: | Dec 15, 1995 | TE: | AP | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 10MG BASE/ML | ||||
| Approval Date: | Dec 15, 1995 | TE: | AP | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 2MG BASE/ML | ||||
| Approval Date: | Dec 15, 1995 | TE: | AP | RLD: | Yes | ||||
Expired US Patents for NDA 020551
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