Package 0338-0703-41
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
0338-0703-41
Digits Only
0338070341
Product NDC
0338-0703
Description
24 BAG in 1 CARTON (0338-0703-41) / 50 mL in 1 BAG
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": ["INTRAVENOUS"], "spl_id": "4cf18d0e-1854-48fb-b711-49b2a3042ae4", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["092ddee4-572d-4771-8d95-880cea01097e"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-0703-41) / 50 mL in 1 BAG", "package_ndc": "0338-0703-41", "marketing_start_date": "19891226"}, {"sample": false, "description": "24 BAG in 1 CARTON (0338-0703-48) / 100 mL in 1 BAG", "package_ndc": "0338-0703-48", "marketing_start_date": "19891226"}], "brand_name": "Potassium Chloride", "product_id": "0338-0703_4cf18d0e-1854-48fb-b711-49b2a3042ae4", "dosage_form": "INJECTION, 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": "0338-0703", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "29.8 g/1000mL"}], "application_number": "NDA019904", "marketing_category": "NDA", "marketing_start_date": "19891226", "listing_expiration_date": "20271231"}