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Lidocaine Hydrochloride
Lidocaine Hydrochloride - 50383-781-30 - (Lidocaine Hydrochloride)
Drug Information of Lidocaine Hydrochloride
| Product NDC: | 50383-781 |
| Proprietary Name: | Lidocaine Hydrochloride |
| Non Proprietary Name: | Lidocaine Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Lidocaine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | JELLY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine Hydrochloride
| Product NDC: | 50383-781 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040837 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110323 |
Package Information of Lidocaine Hydrochloride
| Package NDC: | 50383-781-30 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (50383-781-30) > 30 mL in 1 TUBE, WITH APPLICATOR |
NDC Information of Lidocaine Hydrochloride
| NDC Code | 50383-781-30 |
| Proprietary Name | Lidocaine Hydrochloride |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (50383-781-30) > 30 mL in 1 TUBE, WITH APPLICATOR |
| Product NDC | 50383-781 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine Hydrochloride |
| Dosage Form Name | JELLY |
| Route Name | TOPICAL |
| Start Marketing Date | 20110323 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | LIDOCAINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |
