allergy relief d

Product NDC
37808-785
11-digit product format
378080785
Labeler code
37808
Product ID
37808-785_22d7a8b4-abcd-44ce-828c-4a34ab74f660
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine HCl, Pseudoephedrine HCl
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
H E B
Application
ANDA077170
Marketing category
ANDA
Marketing start
2018-01-19
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Active strength
5 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-785ALLERGY RELIEF D (CETIRIZINE HCL, PSEUDOEPHEDRINE HCL) TABLET, EXTENDED RELEASE [H E B]2Legacy NDC20191205_6c9d6958-4ff6-4433-b029-3427bee26ddc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37808-785-533780807855312 BLISTER PACK in 1 CARTON (37808-785-53) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK12 blister pack2018-01-190000-00-00NoNoCurrent
37808-785-623780807856224 BLISTER PACK in 1 CARTON (37808-785-62) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK24 blister pack2018-01-190000-00-00NoNoCurrent