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TRIHEXYPHENIDYL HYDROCHLORIDE
TRIHEXYPHENIDYL HYDROCHLORIDE - 62584-886-01 - (TRIHEXYPHENIDYL HYDROCHLORIDE)
Drug Information of TRIHEXYPHENIDYL HYDROCHLORIDE
| Product NDC: | 62584-886 |
| 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: | 62584-886 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040254 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100112 |
Package Information of TRIHEXYPHENIDYL HYDROCHLORIDE
| Package NDC: | 62584-886-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (62584-886-01) > 10 TABLET in 1 BLISTER PACK (62584-886-11) |
NDC Information of TRIHEXYPHENIDYL HYDROCHLORIDE
| NDC Code | 62584-886-01 |
| Proprietary Name | TRIHEXYPHENIDYL HYDROCHLORIDE |
| Package Description | 10 BLISTER PACK in 1 CARTON (62584-886-01) > 10 TABLET in 1 BLISTER PACK (62584-886-11) |
| Product NDC | 62584-886 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRIHEXYPHENIDYL HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100112 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | TRIHEXYPHENIDYL HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
