Package 21130-856-52
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
21130-856-52
Digits Only
2113085652
Product NDC
21130-856
Description
1 BOTTLE, PLASTIC in 1 CARTON (21130-856-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
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": "3cbea45d-0c9a-4eba-8e4a-60049a013c25", "openfda": {"upc": ["0321130187158"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["3eeb07fe-fcf1-4ea7-b0c2-9cb04f88c041"], "manufacturer_name": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (21130-856-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-856-52", "marketing_start_date": "20231011"}], "brand_name": "Naproxen Sodium", "product_id": "21130-856_3cbea45d-0c9a-4eba-8e4a-60049a013c25", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-856", "generic_name": "Naproxen Sodium", "labeler_name": "Better Living Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20231011", "listing_expiration_date": "20271231"}