Product NDC: | 0054-3545 |
Proprietary Name: | Meperidine Hydrochloride |
Non Proprietary Name: | Meperidine Hydrochloride |
Active Ingredient(s): | 50 mg/5mL & nbsp; Meperidine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-3545 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088744 |
Marketing Category: | ANDA |
Start Marketing Date: | 19850130 |
Package NDC: | 0054-3545-63 |
Package Description: | 500 mL in 1 BOTTLE (0054-3545-63) |
NDC Code | 0054-3545-63 |
Proprietary Name | Meperidine Hydrochloride |
Package Description | 500 mL in 1 BOTTLE (0054-3545-63) |
Product NDC | 0054-3545 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Meperidine Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19850130 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | MEPERIDINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |