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Naropin
Naropin - 63323-287-21 - (ROPIVACAINE HYDROCHLORIDE)
Drug Information of Naropin
| Product NDC: | 63323-287 |
| Proprietary Name: | Naropin |
| Non Proprietary Name: | ROPIVACAINE HYDROCHLORIDE |
| Active Ingredient(s): | 7.5 mg/mL & nbsp; ROPIVACAINE HYDROCHLORIDE |
| Administration Route(s): | EPIDURAL; PERINEURAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naropin
| Product NDC: | 63323-287 |
| 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: | 63323-287-21 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-287-21) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Naropin
| NDC Code | 63323-287-21 |
| Proprietary Name | Naropin |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-287-21) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-287 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ROPIVACAINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | EPIDURAL; PERINEURAL |
| Start Marketing Date | 20110531 |
| Marketing Category Name | NDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | ROPIVACAINE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |
