Product NDC: | 52533-042 |
Proprietary Name: | Meperidine HCl |
Non Proprietary Name: | Meperidine HCl |
Active Ingredient(s): | 10 mg/mL & nbsp; Meperidine HCl |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-042 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120123 |
Package NDC: | 52533-042-04 |
Package Description: | 50 mL in 1 SYRINGE, PLASTIC (52533-042-04) |
NDC Code | 52533-042-04 |
Proprietary Name | Meperidine HCl |
Package Description | 50 mL in 1 SYRINGE, PLASTIC (52533-042-04) |
Product NDC | 52533-042 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Meperidine HCl |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120123 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cantrell Drug Company |
Substance Name | MEPERIDINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |