Package 70518-2590-0

Brand: rabeprazole sodium

Generic: rabeprazole sodium
NDC Package

Package Facts

Identity

Package NDC 70518-2590-0
Digits Only 7051825900
Product NDC 70518-2590
Product ID 70518-2590_4a69aa10-6b5b-07b3-e063-6294a90a7b87
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2590-0)

Marketing

Marketing Status
Marketed Since 2020-02-18
Brand rabeprazole sodium
Generic rabeprazole sodium
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a69aa10-6b5b-07b3-e063-6294a90a7b87", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["63e0b7ca-6b2d-42a9-b9d4-4523b8a20425"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2590-0)", "package_ndc": "70518-2590-0", "marketing_start_date": "20200218"}], "brand_name": "Rabeprazole Sodium", "product_id": "70518-2590_4a69aa10-6b5b-07b3-e063-6294a90a7b87", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70518-2590", "generic_name": "Rabeprazole Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole Sodium", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA208644", "marketing_category": "ANDA", "marketing_start_date": "20200218", "listing_expiration_date": "20271231"}