DRX CHOICE

Product NDC
68163-065
11-digit product format
681630065
Labeler code
68163
Product ID
68163-065_36a9f110-51f5-54e9-e063-6294a90a921f
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Raritan Pharmaceuticals Inc.
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-05-16
Substance
ACETAMINOPHEN
Active strength
325 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
DRX CHOICE
Brand name suffix
Regular Strength
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN325 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii362O9ITL9D
Rxcui313782

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68163-065-60DRX CHOICERegular Strength60 in 1 BOTTLETABLET, FILM COATED601

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313782acetaminophen 325 MG Oral TabletPSN8bacb24a-24d0-4175-b3e0-05efb5f5d3731
313782acetaminophen 325 MG Oral TabletSCD8bacb24a-24d0-4175-b3e0-05efb5f5d3731
313782APAP 325 MG Oral TabletSY8bacb24a-24d0-4175-b3e0-05efb5f5d3731

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
68163-065-606816300656060 TABLET, FILM COATED in 1 BOTTLE (68163-065-60) 2025-05-16NoNoCurrent