diphenhydramine hydrochloride

Product NDC
0185-0649
11-digit product format
001850649
Labeler code
0185
Product ID
0185-0649_419f717e-45ed-4cb5-9d35-a6d43058cd70
Type
HUMAN OTC DRUG
Nonproprietary name
diphenhydramine hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Eon Labs, Inc.
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2000-05-01
Marketing end
2021-06-30
Substance
DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
50 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0185-0649-01EA - Each0185-06490b635ece-7e87-4037-b7fc-508fc77e94e212012-07-24
0185-0649-10EA - Each0185-0649eb455c49-62aa-4d91-93f9-1813351fa88812012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020477diphenhydrAMINE HCl 50 MG Oral CapsulePSN8975a041-76dd-4c5e-aa83-e1021d55a0841
1020477diphenhydramine hydrochloride 50 MG Oral CapsuleSCD8975a041-76dd-4c5e-aa83-e1021d55a0841
1020477diphenhydramine HCl 50 MG Oral CapsuleSY8975a041-76dd-4c5e-aa83-e1021d55a0841

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0185-0649-0100185064901100 CAPSULE in 1 BOTTLE (0185-0649-01) 100 capsule2000-05-012021-04-30NoNoCurrent
0185-0649-10001850649101000 CAPSULE in 1 BOTTLE (0185-0649-10) 1000 capsule2000-05-012021-06-30NoNoCurrent