Package 27854-701-01

Brand: ana-dent pain relief

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 27854-701-01
Digits Only 2785470101
Product NDC 27854-701
Description

1 BOTTLE in 1 CARTON (27854-701-01) / 24 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-05-15
Brand ana-dent pain relief
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5ac02446-13da-43d5-9647-fe469294acec", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["04721306-2850-4e0a-9dd9-7cabb575f3c7"], "manufacturer_name": ["Belmora LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (27854-701-01)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "27854-701-01", "marketing_start_date": "20200515"}], "brand_name": "Ana-Dent PAIN RELIEF", "product_id": "27854-701_5ac02446-13da-43d5-9647-fe469294acec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "27854-701", "generic_name": "Naproxen Sodium", "labeler_name": "Belmora LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ana-Dent PAIN RELIEF", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA205497", "marketing_category": "ANDA", "marketing_start_date": "20200515", "listing_expiration_date": "20261231"}