EQUATE MENSTRUAL PAIN RELIEF

Product NDC
79903-420
11-digit product format
799030420
Labeler code
79903
Product ID
79903-420_d4303948-b989-4e0a-ace6-3ac5643e68e1
Type
HUMAN OTC DRUG
Nonproprietary name
acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
WALMART INC.
Application
ANDA075077
Marketing category
ANDA
Marketing start
2026-04-29
Substance
ACETAMINOPHEN
Active strength
650 mg/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
EQUATE MENSTRUAL 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 Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-420-20EQUATE MENSTRUAL PAIN RELIEF1 in 1 CARTONTABLET, FILM COATED, EXTENDED RE12
79903-420-20EQUATE MENSTRUAL PAIN RELIEF20 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE202

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1148399acetaminophen 650 MG 8HR Extended Release Oral TabletPSNe387ae77-27e9-455a-b708-43288411b2c12
11483998 HR acetaminophen 650 MG Extended Release Oral TabletSCDe387ae77-27e9-455a-b708-43288411b2c12
11483998 HR APAP 650 MG Extended Release Oral TabletSYe387ae77-27e9-455a-b708-43288411b2c12
1148399acetaminophen 650 MG 8 HR Extended Release Oral TabletSYe387ae77-27e9-455a-b708-43288411b2c12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79903-420-20799030420201 BOTTLE in 1 CARTON (79903-420-20) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE1 bottle2026-04-29NoNoCurrent