Package 55111-129-05

Brand: ranitidine hydrochloride

Generic: ranitidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55111-129-05
Digits Only 5511112905
Product NDC 55111-129
Description

500 CAPSULE in 1 BOTTLE (55111-129-05)

Marketing

Marketing Status
Marketed Since 2001-01-12
Brand ranitidine hydrochloride
Generic ranitidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9741e6f4-a2dc-7543-1138-da97eafe11bd", "openfda": {"unii": ["BK76465IHM"], "rxcui": ["198190", "198192"], "spl_set_id": ["7bf94bf7-fa11-70be-9f65-fe26a3db5a63"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (55111-129-05)", "package_ndc": "55111-129-05", "marketing_start_date": "20010112"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (55111-129-60)", "package_ndc": "55111-129-60", "marketing_start_date": "20010112"}], "brand_name": "Ranitidine Hydrochloride", "product_id": "55111-129_9741e6f4-a2dc-7543-1138-da97eafe11bd", "dosage_form": "CAPSULE", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "55111-129", "generic_name": "Ranitidine Hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ranitidine Hydrochloride", "active_ingredients": [{"name": "RANITIDINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA075742", "marketing_category": "ANDA", "marketing_start_date": "20010112", "listing_expiration_date": "20261231"}