Package 27854-700-10

Brand: flanax pain reliever/fever reducer

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 27854-700-10
Digits Only 2785470010
Product NDC 27854-700
Description

1 BOTTLE in 1 CARTON (27854-700-10) / 10 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-05-15
Brand flanax pain reliever/fever reducer
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4215c852-11ed-4b06-b132-3674265078e3", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["a93e4966-9dd3-40ba-b7d6-6ca8fef229c6"], "manufacturer_name": ["Belmora LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (27854-700-01)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "27854-700-01", "marketing_start_date": "20200515"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (27854-700-10)  / 10 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "27854-700-10", "marketing_start_date": "20200515"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (27854-700-99)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "27854-700-99", "marketing_start_date": "20200515"}], "brand_name": "Flanax Pain Reliever/Fever Reducer", "product_id": "27854-700_4215c852-11ed-4b06-b132-3674265078e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "27854-700", "generic_name": "Naproxen sodium", "labeler_name": "Belmora LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Flanax Pain Reliever/Fever Reducer", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA205497", "marketing_category": "ANDA", "marketing_start_date": "20200515", "listing_expiration_date": "20261231"}