Product NDC: | 0121-0658 |
Proprietary Name: | Trihexyphenidyl Hydrochloride |
Non Proprietary Name: | Trihexyphenidyl Hydrochloride |
Active Ingredient(s): | 2 mg/5mL & nbsp; Trihexyphenidyl Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0121-0658 |
Labeler Name: | Pharmaceutical Associates, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040177 |
Marketing Category: | ANDA |
Start Marketing Date: | 19970515 |
Package NDC: | 0121-0658-16 |
Package Description: | 473 mL in 1 BOTTLE (0121-0658-16) |
NDC Code | 0121-0658-16 |
Proprietary Name | Trihexyphenidyl Hydrochloride |
Package Description | 473 mL in 1 BOTTLE (0121-0658-16) |
Product NDC | 0121-0658 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Trihexyphenidyl Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19970515 |
Marketing Category Name | ANDA |
Labeler Name | Pharmaceutical Associates, Inc. |
Substance Name | TRIHEXYPHENIDYL HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |