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Trihexyphenidyl Hydrochloride
Trihexyphenidyl Hydrochloride - 16571-160-11 - (Trihexyphenidyl Hydrochloride)
Drug Information of Trihexyphenidyl Hydrochloride
| Product NDC: | 16571-160 |
| Proprietary Name: | Trihexyphenidyl Hydrochloride |
| Non Proprietary Name: | Trihexyphenidyl Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Trihexyphenidyl Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trihexyphenidyl Hydrochloride
| Product NDC: | 16571-160 |
| Labeler Name: | Pack Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091630 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101117 |
Package Information of Trihexyphenidyl Hydrochloride
| Package NDC: | 16571-160-11 |
| Package Description: | 1000 TABLET in 1 BOTTLE (16571-160-11) |
NDC Information of Trihexyphenidyl Hydrochloride
| NDC Code | 16571-160-11 |
| Proprietary Name | Trihexyphenidyl Hydrochloride |
| Package Description | 1000 TABLET in 1 BOTTLE (16571-160-11) |
| Product NDC | 16571-160 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Trihexyphenidyl Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101117 |
| Marketing Category Name | ANDA |
| Labeler Name | Pack Pharmaceuticals, LLC |
| Substance Name | TRIHEXYPHENIDYL HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
