Product NDC: | 42023-142 |
Proprietary Name: | Trimethobenzamide Hydrochloride |
Non Proprietary Name: | trimethobenzamide hydrochloride |
Active Ingredient(s): | 100 mg/mL & nbsp; trimethobenzamide hydrochloride |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42023-142 |
Labeler Name: | JHP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017530 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20120601 |
Package NDC: | 42023-142-01 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (42023-142-01) > 20 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 42023-142-01 |
Proprietary Name | Trimethobenzamide Hydrochloride |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (42023-142-01) > 20 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 42023-142 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | trimethobenzamide hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20120601 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | JHP Pharmaceuticals, LLC |
Substance Name | TRIMETHOBENZAMIDE HYDROCHLORIDE |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Antiemetic [EPC],Emesis Suppression [PE] |