Naropin - 63323-288-11 - (ROPIVACAINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Naropin

Product NDC: 63323-288
Proprietary Name: Naropin
Non Proprietary Name: ROPIVACAINE HYDROCHLORIDE
Active Ingredient(s): 10    mg/mL & nbsp;   ROPIVACAINE HYDROCHLORIDE
Administration Route(s): EPIDURAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Naropin

Product NDC: 63323-288
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020533
Marketing Category: NDA
Start Marketing Date: 20110531

Package Information of Naropin

Package NDC: 63323-288-11
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-288-11) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Naropin

NDC Code 63323-288-11
Proprietary Name Naropin
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-288-11) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-288
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ROPIVACAINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name EPIDURAL
Start Marketing Date 20110531
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name ROPIVACAINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE]

Complete Information of Naropin


General Information