Package 80725-243-30

Brand: aciphex

Generic: rabeprazole sodium
NDC Package

Package Facts

Identity

Package NDC 80725-243-30
Digits Only 8072524330
Product NDC 80725-243
Product ID 80725-243_cc6cb214-ac28-4c8b-9b57-7635ef896038
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (80725-243-30)

Marketing

Marketing Status
Marketed Since 2023-12-01
Brand aciphex
Generic rabeprazole sodium
Sample Package No

Linked Drug Pages (1)

Aciphex ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cc6cb214-ac28-4c8b-9b57-7635ef896038", "openfda": {"upc": ["0380725243303"], "unii": ["3L36P16U4R"], "rxcui": ["854868", "854870"], "spl_set_id": ["1eb38279-0237-4967-be7a-c53a826c1138"], "manufacturer_name": ["Waylis Therapeutics LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (80725-243-30)", "package_ndc": "80725-243-30", "marketing_start_date": "20231201"}], "brand_name": "Aciphex", "product_id": "80725-243_cc6cb214-ac28-4c8b-9b57-7635ef896038", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80725-243", "generic_name": "rabeprazole sodium", "labeler_name": "Waylis Therapeutics LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aciphex", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "NDA020973", "marketing_category": "NDA", "marketing_start_date": "20220515", "listing_expiration_date": "20271231"}