FDA.reportPublic FDA data

14803-903-00

Product NDC
14803-903
Requested package NDC
14803-903-00
11-digit product format
148030903
Labeler code
14803
Product ID
14803-903_5127ac89-3e07-5966-e063-6394a90a11db
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydramine Hydrochloride
Dosage form
CAPSULE
Marketing category
DRUG FOR FURTHER PROCESSING
Marketing start
2020-11-26
Substance
DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
50 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 packagepackage14803-90314803-903-00UNFINISHEDActive 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
DIPHENHYDRAMINE HYDROCHLORIDE50 mg/1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startStatus
14803-903-001480309030040500 CAPSULE in 1 DRUM (14803-903-00)40500 capsule26-NOV-20Current