Trihexyphenidyl Hydrochloride

Product NDC
70518-3288
11-digit product format
705183288
Labeler code
70518
Product ID
70518-3288_d3080a23-f83b-414a-e053-2a95a90a1f34
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trihexyphenidyl Hydrochloride
Dosage form
SYRUP
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA040251
Marketing category
ANDA
Marketing start
2021-12-10
Marketing end
0000-00-00
Substance
TRIHEXYPHENIDYL HYDROCHLORIDE
Active strength
2 mg/5mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-3288-02023-03-23C16284748780-1f386c649-aa7e-0266-e053-dadaa90a7c1a23af0edb-1ada-4d49-b1d0-896deae99a83
70518-3288-02023-01-30C16284748780-1f386c649-aa7e-0266-e053-dadaa90a7c1a23af0edb-1ada-4d49-b1d0-896deae99a83

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70518-3288-07051832880010 CUP, UNIT-DOSE in 1 BOX (70518-3288-0) > 12.5 mL in 1 CUP, UNIT-DOSE (70518-3288-1) 2021-12-100000-00-00NoNoCurrent