Package 41520-349-82

Brand: care one naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 41520-349-82
Digits Only 4152034982
Product NDC 41520-349
Description

200 TABLET, FILM COATED in 1 BOTTLE (41520-349-82)

Marketing

Marketing Status
Marketed Since 2016-06-13
Brand care one naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f162d9b0-e842-42ea-bfb5-78f450cbb772", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["88812af7-89ca-449b-9513-20c284543d0e"], "manufacturer_name": ["American Sales Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (41520-349-82)", "package_ndc": "41520-349-82", "marketing_start_date": "20160613"}], "brand_name": "Care One Naproxen Sodium", "product_id": "41520-349_f162d9b0-e842-42ea-bfb5-78f450cbb772", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41520-349", "generic_name": "Naproxen sodium", "labeler_name": "American Sales Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Care One Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20160613", "listing_expiration_date": "20261231"}