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Lidocaine HCl - Hydrocortisone Acetate
Lidocaine HCl - Hydrocortisone Acetate - 59088-838-20 - (Lidocaine HCl and Hydrocortisone Acetate)
Drug Information of Lidocaine HCl - Hydrocortisone Acetate
| Product NDC: | 59088-838 |
| Proprietary Name: | Lidocaine HCl - Hydrocortisone Acetate |
| Non Proprietary Name: | Lidocaine HCl and Hydrocortisone Acetate |
| Active Ingredient(s): | 25; 30 mg/g; mg/g & nbsp; Lidocaine HCl and Hydrocortisone Acetate |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lidocaine HCl - Hydrocortisone Acetate
| Product NDC: | 59088-838 |
| Labeler Name: | PureTek Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110622 |
Package Information of Lidocaine HCl - Hydrocortisone Acetate
| Package NDC: | 59088-838-20 |
| Package Description: | 20 TUBE in 1 KIT (59088-838-20) > 7 g in 1 TUBE (59088-838-01) |
NDC Information of Lidocaine HCl - Hydrocortisone Acetate
| NDC Code | 59088-838-20 |
| Proprietary Name | Lidocaine HCl - Hydrocortisone Acetate |
| Package Description | 20 TUBE in 1 KIT (59088-838-20) > 7 g in 1 TUBE (59088-838-01) |
| Product NDC | 59088-838 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lidocaine HCl and Hydrocortisone Acetate |
| Dosage Form Name | GEL |
| Route Name | RECTAL |
| Start Marketing Date | 20110622 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | PureTek Corporation |
| Substance Name | HYDROCORTISONE ACETATE; LIDOCAINE HYDROCHLORIDE |
| Strength Number | 25; 30 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
