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 PACK2023-08-11NoHistorical
70677-1020-22 BLISTER PACK in 1 CARTON (70677-1020-2) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK2024-10-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Allergy relief-DSTRATEGIC SOURCING SERVICES LLC | Sun Pharmaceutical Industries Limited2024-10-03HUMAN OTC DRUG LABEL3