Pamprin

Product NDC
71687-3009
11-digit product format
716873009
Labeler code
71687
Product ID
71687-3009_42f18430-4323-4a63-e063-6394a90a0382
Type
HUMAN OTC DRUG
Nonproprietary name
Pamabrom
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Focus Consumer Healthcare, LLC
Application
M027
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-31
Substance
PAMABROM
Active strength
50 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
Pamprin
Brand name suffix
Bloat
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PAMABROM50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiUA8U0KJM72
Rxcui199158

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71687-3009-1PamprinBloat1 in 1 CARTONTABLET, FILM COATED11
71687-3009-1PamprinBloat30 in 1 BOTTLETABLET, FILM COATED301

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199158pamabrom 50 MG Oral TabletPSN42f1846d-2d57-5221-e063-6394a90a3a9f1
199158pamabrom 50 MG Oral TabletSCD42f1846d-2d57-5221-e063-6394a90a3a9f1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71687-3009-1716873009011 BOTTLE in 1 CARTON (71687-3009-1) / 30 TABLET, FILM COATED in 1 BOTTLE1 bottle2025-12-31NoNoCurrent