FDA.reportPublic FDA data

Dicopanol

Product NDC
70332-103
11-digit product format
703320103
Labeler code
70332
Product ID
70332-103_28c7a185-4081-1448-e054-00144ff8d46c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Diphenhydramine Hydrochloride
Dosage form
KIT
Route
ORAL
Labeler
California Pharmaceuticals LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2016-01-01
Marketing end
0000-00-00
Active strength
0
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70332-103-012020-01-31C16284748780-19d75b9d0-27a9-f424-e053-dadaa90a57ceDicopanol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70332-103-01Dicopanol1 in 1 KITKIT12

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70332-103-01ML - Milliliter70332-103d153a13f-562a-4c0c-8585-688db565490112016-09-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70332-103DICOPANOL (DIPHENHYDRAMINE HYDROCHLORIDE) KIT [CALIFORNIA PHARMACEUTICALS LLC]2Legacy NDC, 1 package rows20160108_271bfbb6-4996-500a-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
70332-103-01703320103011 in 1 KITHistorical