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Lidocaine
Lidocaine - 21695-826-35 - (Lidocaine)
Drug Information of Lidocaine
| Product NDC: | 21695-826 |
| Proprietary Name: | Lidocaine |
| Non Proprietary Name: | Lidocaine |
| Active Ingredient(s): | 50 mg/g & nbsp; Lidocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine
| Product NDC: | 21695-826 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080198 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19720630 |
Package Information of Lidocaine
| Package NDC: | 21695-826-35 |
| Package Description: | 35 g in 1 TUBE (21695-826-35) |
NDC Information of Lidocaine
| NDC Code | 21695-826-35 |
| Proprietary Name | Lidocaine |
| Package Description | 35 g in 1 TUBE (21695-826-35) |
| Product NDC | 21695-826 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19720630 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | LIDOCAINE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] |
