Allergy relief-D

Product NDC
70677-1020
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
STRATEGIC SOURCING SERVICES LLC
Application
ANDA090922
Marketing category
ANDA
Substance
CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70677-1020-14 BLISTER PACK in 1 CARTON (70677-1020-1) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK20230811NoHistorical
70677-1020-22 BLISTER PACK in 1 CARTON (70677-1020-2) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK20241004NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
97997887-9cba-48f8-abcd-fdb86829459cAllergy relief-DSTRATEGIC SOURCING SERVICES LLC | Sun Pharmaceutical Industries Limited2024-10-03HUMAN OTC DRUG LABEL3