Package 62207-761-43
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
62207-761-43
Digits Only
6220776143
Product NDC
62207-761
Description
100 TABLET, FILM COATED in 1 BOTTLE (62207-761-43)
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": "f4026a0a-c9cd-3850-e053-2995a90a459c", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["95ba1722-60ed-4a83-9f26-50c4de8cf180"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (62207-761-42)", "package_ndc": "62207-761-42", "marketing_start_date": "20110930"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62207-761-43)", "package_ndc": "62207-761-43", "marketing_start_date": "20110930"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62207-761-47)", "package_ndc": "62207-761-47", "marketing_start_date": "20110930"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62207-761-49)", "package_ndc": "62207-761-49", "marketing_start_date": "20110930"}], "brand_name": "Naproxen Sodium", "product_id": "62207-761_f4026a0a-c9cd-3850-e053-2995a90a459c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "62207-761", "generic_name": "Naproxen Sodium", "labeler_name": "Granules India Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20110930", "listing_expiration_date": "20261231"}