Package 55910-500-82
Brand: dg health naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
55910-500-82
Digits Only
5591050082
Product NDC
55910-500
Description
1 BOTTLE in 1 CARTON (55910-500-82) / 200 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
dg health 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": "0833bb77-1309-4ed7-ad4a-9b1044fb0799", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["3ca9ce63-39f4-4ba9-b464-d048fd8e67c0"], "manufacturer_name": ["Dolgencorp Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-500-82) / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55910-500-82", "marketing_start_date": "20170905"}], "brand_name": "dg health naproxen sodium", "product_id": "55910-500_0833bb77-1309-4ed7-ad4a-9b1044fb0799", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55910-500", "generic_name": "Naproxen Sodium", "labeler_name": "Dolgencorp Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dg health naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20131121", "listing_expiration_date": "20261231"}