Package 49483-609-01

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 49483-609-01
Digits Only 4948360901
Product NDC 49483-609
Product ID 49483-609_cbf198fe-25e4-694c-e053-2995a90aae22
Description

100 TABLET, FILM COATED in 1 BOTTLE (49483-609-01)

Marketing

Marketing Status
Marketed Since 2016-03-28
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": "cbf198fe-25e4-694c-e053-2995a90aae22", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["17ecaee0-c1c6-4360-81c1-d6afe50b9b27"], "manufacturer_name": ["TIME CAP LABORATORIES, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6500 TABLET, FILM COATED in 1 BAG (49483-609-00)", "package_ndc": "49483-609-00", "marketing_start_date": "20160328"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (49483-609-01)", "package_ndc": "49483-609-01", "marketing_start_date": "20160328"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (49483-609-05)", "package_ndc": "49483-609-05", "marketing_start_date": "20160328"}], "brand_name": "NAPROXEN SODIUM", "product_id": "49483-609_cbf198fe-25e4-694c-e053-2995a90aae22", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49483-609", "generic_name": "NAPROXEN SODIUM", "labeler_name": "TIME CAP LABORATORIES, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NAPROXEN SODIUM", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20160328", "listing_expiration_date": "20261231"}