FDA.reportPublic FDA data

14803-013-00

Product NDC
14803-013
Requested package NDC
14803-013-00
11-digit product format
148030013
Labeler code
14803
Product ID
14803-013_4ac18e0b-f6d6-caf4-e063-6294a90a7a34
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Marketing category
DRUG FOR FURTHER PROCESSING
Marketing start
2024-03-07
Substance
ACETAMINOPHEN
Active strength
325 mg/1
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
unfinished packagepackage14803-01314803-013-00UNFINISHEDActive or certified unfinished drug listing2026-10-16

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
No
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN325 mg/1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startStatus
14803-013-001480300130047000 TABLET in 1 BOX (14803-013-00)47000 tablet01-MAR-25Current