Product NDC: | 54868-3559 |
Proprietary Name: | Meperidine Hydrochloride |
Non Proprietary Name: | Meperidine Hydrochloride |
Active Ingredient(s): | 50 mg/mL & nbsp; Meperidine Hydrochloride |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-3559 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080455 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100304 |
Package NDC: | 54868-3559-1 |
Package Description: | 25 VIAL in 1 PACKAGE (54868-3559-1) > 1 mL in 1 VIAL |
NDC Code | 54868-3559-1 |
Proprietary Name | Meperidine Hydrochloride |
Package Description | 25 VIAL in 1 PACKAGE (54868-3559-1) > 1 mL in 1 VIAL |
Product NDC | 54868-3559 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Meperidine Hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20100304 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | MEPERIDINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |