NAROPIN - 63323-285-13 - (ROPIVACAINE HYDROCHLORIDE MONOHYDRATE)

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Drug Information of NAROPIN

Product NDC: 63323-285
Proprietary Name: NAROPIN
Non Proprietary Name: ROPIVACAINE HYDROCHLORIDE MONOHYDRATE
Active Ingredient(s): 2    mg/mL & nbsp;   ROPIVACAINE HYDROCHLORIDE MONOHYDRATE
Administration Route(s): EPIDURAL; INFILTRATION
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of NAROPIN

Product NDC: 63323-285
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020533
Marketing Category: NDA
Start Marketing Date: 20090804

Package Information of NAROPIN

Package NDC: 63323-285-13
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-285-13) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of NAROPIN

NDC Code 63323-285-13
Proprietary Name NAROPIN
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-285-13) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-285
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ROPIVACAINE HYDROCHLORIDE MONOHYDRATE
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL; INFILTRATION
Start Marketing Date 20090804
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name ROPIVACAINE HYDROCHLORIDE MONOHYDRATE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of NAROPIN


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