Package 37808-106-08

Brand: allergy relief

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 37808-106-08
Digits Only 3780810608
Product NDC 37808-106
Description

1 BOTTLE in 1 CARTON (37808-106-08) / 120 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-04-12
Brand allergy relief
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e05caf8-84cf-478f-9401-762f51c9e796", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["fdd3f9a0-b4be-498a-b8e0-1a9740399736"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-106-08)  / 120 mL in 1 BOTTLE", "package_ndc": "37808-106-08", "marketing_start_date": "20180412"}], "brand_name": "Allergy Relief", "product_id": "37808-106_3e05caf8-84cf-478f-9401-762f51c9e796", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-106", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA201546", "marketing_category": "ANDA", "marketing_start_date": "20110520", "listing_expiration_date": "20261231"}