Package 69729-137-14

Brand: pentrexcilina day time

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69729-137-14
Digits Only 6972913714
Product NDC 69729-137
Product ID 69729-137_26f56cb7-be59-a0c2-e063-6294a90a15fa
Description

14 TABLET in 1 BOTTLE (69729-137-14)

Marketing

Marketing Status
Marketed Since 2024-11-15
Brand pentrexcilina day time
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Pentrexcilina Day time ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "26f56cb7-be59-a0c2-e063-6294a90a15fa", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["26f56cb7-be58-a0c2-e063-6294a90a15fa"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (69729-137-14)", "package_ndc": "69729-137-14", "marketing_start_date": "20241115"}], "brand_name": "Pentrexcilina Day time", "product_id": "69729-137_26f56cb7-be59-a0c2-e063-6294a90a15fa", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69729-137", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pentrexcilina Day time", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20241115", "listing_expiration_date": "20261231"}