Product NDC: | 58980-822 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | 5.31 mL/177mL & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58980-822 |
Labeler Name: | Stratus Pharamceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120301 |
Package NDC: | 58980-822-60 |
Package Description: | 1 BOTTLE in 1 BOX (58980-822-60) > 177 mL in 1 BOTTLE |
NDC Code | 58980-822-60 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | 1 BOTTLE in 1 BOX (58980-822-60) > 177 mL in 1 BOTTLE |
Product NDC | 58980-822 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120301 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Stratus Pharamceuticals |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | 5.31 |
Strength Unit | mL/177mL |
Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |