Package 70771-1600-0

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 70771-1600-0
Digits Only 7077116000
Product NDC 70771-1600
Description

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-0)

Marketing

Marketing Status
Marketed Since 2022-02-03
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c6b38e40-cd5a-41ed-92d6-eb25e9c0c725", "openfda": {"upc": ["0370771160013", "0370771159918"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["099c3a36-f460-4191-80e5-0c4153a5c713"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-0)", "package_ndc": "70771-1600-0", "marketing_start_date": "20220203"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-1)", "package_ndc": "70771-1600-1", "marketing_start_date": "20220203"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-5)", "package_ndc": "70771-1600-5", "marketing_start_date": "20220203"}], "brand_name": "Potassium Chloride", "product_id": "70771-1600_c6b38e40-cd5a-41ed-92d6-eb25e9c0c725", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "70771-1600", "generic_name": "Potassium Chloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA210395", "marketing_category": "ANDA", "marketing_start_date": "20220203", "listing_expiration_date": "20261231"}