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NDC 70518-3268-00 Trihexyphenidyl Hydrochloride 2 mg/5mL Details
Trihexyphenidyl Hydrochloride 2 mg/5mL
Trihexyphenidyl Hydrochloride is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is TRIHEXYPHENIDYL HYDROCHLORIDE.
MedlinePlus Drug Summary
Trihexyphenidyl is used along with other medications to treat the symptoms of Parkinson's disease (PD; a disorder of the nervous system that causes difficulties with movement, muscle control, and balance) and to control extrapyramidal symptoms (tremor, slurred speech) caused by certain medications. Trihexyphenidyl is in a class of medications called antimuscarinics. It works by relaxing muscles and nerve impulses that control the function of muscles.
Related Packages: 70518-3268-00Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Trihexyphenidyl
Product Information
NDC | 70518-3268 |
---|---|
Product ID | 70518-3268_fb7ecf67-7f95-b3c3-e053-6294a90a88e7 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Trihexyphenidyl Hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Trihexyphenidyl Hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | SOLUTION |
Route | ORAL |
Active Ingredient Strength | 2 |
Active Ingredient Units | mg/5mL |
Substance Name | TRIHEXYPHENIDYL HYDROCHLORIDE |
Labeler Name | REMEDYREPACK INC. |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA040177 |
Listing Certified Through | 2024-12-31 |
Package
NDC 70518-3268-00 (70518326800)
NDC Package Code | 70518-3268-0 |
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Billing NDC | 70518326800 |
Package | 10 CUP, UNIT-DOSE in 1 BOX (70518-3268-0) / 12.5 mL in 1 CUP, UNIT-DOSE (70518-3268-1) |
Marketing Start Date | 2021-11-15 |
NDC Exclude Flag | N |
Pricing Information | N/A |