Package 27854-170-01
Brand: anadent
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
27854-170-01
Digits Only
2785417001
Product NDC
27854-170
Description
1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
anadent
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "16b93df8-98f1-4fad-96a7-f814ff0c084a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["236674db-da4d-415c-a160-7086eaf5bff5"], "manufacturer_name": ["Belmora LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "27854-170-01", "marketing_start_date": "20170123"}], "brand_name": "AnaDent", "product_id": "27854-170_16b93df8-98f1-4fad-96a7-f814ff0c084a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "27854-170", "generic_name": "Naproxen Sodium", "labeler_name": "Belmora LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AnaDent", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20170123", "listing_expiration_date": "20261231"}