Good Sense Pain Relief

Product NDC
0113-0044
11-digit product format
001130044
Labeler code
0113
Product ID
0113-0044_694143e8-301e-4825-91e7-716d1f9b3a14
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
L. Perrigo Company
Application
ANDA075077
Marketing category
ANDA
Marketing start
2017-05-09
Marketing end
2024-02-29
Substance
ACETAMINOPHEN
Active strength
650 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Additional Listing Data#

Finished product
Yes
Brand name base
Good Sense Pain Relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN650 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii362O9ITL9D
Rxcui1148399

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0113-0044-71EA - Each0113-004479a7573b-e110-4f85-bee5-c13273ae80a712022-03-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0113-0044-71001130044711 BOTTLE in 1 CARTON (0113-0044-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE1 bottle2017-05-090000-00-00NoNoCurrent
0113-0044-78001130044781 BOTTLE in 1 CARTON (0113-0044-78) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0113-0044-00)1 bottle2026-04-300Current