Package 43598-183-31
Brand: cetirizine hydrochloride
Generic: cetirizine hydrochloride tabletsPackage Facts
Identity
Package NDC
43598-183-31
Digits Only
4359818331
Product NDC
43598-183
Description
300 TABLET, FILM COATED in 1 BOTTLE (43598-183-31)
Marketing
Marketing Status
Brand
cetirizine hydrochloride
Generic
cetirizine hydrochloride tablets
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9b5f0b11-2f7f-0cb0-0ce7-c06c0b85c5c7", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["206ab55a-3720-6205-d710-6e7953571418"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (43598-183-31)", "package_ndc": "43598-183-31", "marketing_start_date": "20240401"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43598-183-55)", "package_ndc": "43598-183-55", "marketing_start_date": "20231101"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "43598-183_9b5f0b11-2f7f-0cb0-0ce7-c06c0b85c5c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "43598-183", "generic_name": "Cetirizine Hydrochloride Tablets", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078343", "marketing_category": "ANDA", "marketing_start_date": "20181217", "listing_expiration_date": "20261231"}