Package 27808-168-01
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
27808-168-01
Digits Only
2780816801
Product NDC
27808-168
Description
473 mL in 1 BOTTLE (27808-168-01)
Marketing
Marketing Status
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": "f15016a3-b389-4ca4-9127-f6f438254434", "openfda": {"upc": ["0327808169013", "0327808168016"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["159ddd0b-847e-4ecc-b3b2-9634cbb4dfa9"], "manufacturer_name": ["Tris Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (27808-168-01)", "package_ndc": "27808-168-01", "marketing_start_date": "20221230"}], "brand_name": "Potassium Chloride", "product_id": "27808-168_f15016a3-b389-4ca4-9127-f6f438254434", "dosage_form": "SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "27808-168", "generic_name": "Potassium Chloride", "labeler_name": "Tris Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA214076", "marketing_category": "ANDA", "marketing_start_date": "20220126", "listing_expiration_date": "20261231"}