Package 27854-160-01

Brand: flanax

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 27854-160-01
Digits Only 2785416001
Product NDC 27854-160
Description

1 BOTTLE, PLASTIC in 1 CARTON (27854-160-01) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2018-01-15
Brand flanax
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15256b57-2263-447e-9a11-f3f8f7edd6c3", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["2c099d45-f03a-4161-a6af-8fe5965f2748"], "manufacturer_name": ["Belmora LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (27854-160-01)  / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "27854-160-01", "marketing_start_date": "20180115"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (27854-160-24)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "27854-160-24", "marketing_start_date": "20180115"}], "brand_name": "Flanax", "product_id": "27854-160_15256b57-2263-447e-9a11-f3f8f7edd6c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "27854-160", "generic_name": "Naproxen Sodium", "labeler_name": "Belmora LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Flanax", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20271231"}