Package 37808-713-79

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 37808-713-79
Digits Only 3780871379
Product NDC 37808-713
Product ID 37808-713_6ee71bc8-3819-4e08-85f5-9557df90ad5a
Description

400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)

Marketing

Marketing Status
Marketed Since 2017-10-03
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

naproxen sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6ee71bc8-3819-4e08-85f5-9557df90ad5a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["b5dcf3df-2628-49c7-9d96-64886bebe631"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)", "package_ndc": "37808-713-79", "marketing_start_date": "20171003"}], "brand_name": "naproxen sodium", "product_id": "37808-713_6ee71bc8-3819-4e08-85f5-9557df90ad5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-713", "generic_name": "Naproxen Sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20171003", "listing_expiration_date": "20261231"}