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Lidocaine and Prilocaine
Lidocaine and Prilocaine - 50383-667-30 - (Lidocaine and Prilocaine)
Drug Information of Lidocaine and Prilocaine
| Product NDC: | 50383-667 |
| Proprietary Name: | Lidocaine and Prilocaine |
| Non Proprietary Name: | Lidocaine and Prilocaine |
| Active Ingredient(s): | 25; 25 mg/g; mg/g & nbsp; Lidocaine and Prilocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine and Prilocaine
| Product NDC: | 50383-667 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076290 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030925 |
Package Information of Lidocaine and Prilocaine
| Package NDC: | 50383-667-30 |
| Package Description: | 1 TUBE in 1 CARTON (50383-667-30) > 30 g in 1 TUBE |
NDC Information of Lidocaine and Prilocaine
| NDC Code | 50383-667-30 |
| Proprietary Name | Lidocaine and Prilocaine |
| Package Description | 1 TUBE in 1 CARTON (50383-667-30) > 30 g in 1 TUBE |
| Product NDC | 50383-667 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine and Prilocaine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20030925 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | LIDOCAINE; PRILOCAINE |
| Strength Number | 25; 25 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE],Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |
