Package 43353-162-94

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 43353-162-94
Digits Only 4335316294
Product NDC 43353-162
Description

360 TABLET in 1 BOTTLE, PLASTIC (43353-162-94)

Marketing

Marketing Status
Marketed Since 2016-02-22
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36d1abdc-f28b-4c0d-98ea-07718706c695", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["15605a6d-6c90-47d5-9d1f-f66a3f27d5fc"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43353-162-53)", "package_ndc": "43353-162-53", "marketing_start_date": "20160330"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43353-162-60)", "package_ndc": "43353-162-60", "marketing_start_date": "20160222"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (43353-162-70)", "package_ndc": "43353-162-70", "marketing_start_date": "20160222"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (43353-162-80)", "package_ndc": "43353-162-80", "marketing_start_date": "20160330"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE, PLASTIC (43353-162-85)", "package_ndc": "43353-162-85", "marketing_start_date": "20160302"}, {"sample": false, "description": "360 TABLET in 1 BOTTLE, PLASTIC (43353-162-94)", "package_ndc": "43353-162-94", "marketing_start_date": "20160222"}], "brand_name": "SODIUM BICARBONATE", "product_id": "43353-162_36d1abdc-f28b-4c0d-98ea-07718706c695", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "43353-162", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "part331", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20150501", "listing_expiration_date": "20261231"}