Package 21130-690-05

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 21130-690-05
Digits Only 2113069005
Product NDC 21130-690
Description

1 BOTTLE in 1 CARTON (21130-690-05) / 50 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-06-13
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": "fe75f23c-9c5e-03a4-e053-6294a90a696d", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f2c06861-0322-93ed-e053-2995a90a5902"], "manufacturer_name": ["BETTER LIVING BRANDS LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-690-05)  / 50 TABLET in 1 BOTTLE", "package_ndc": "21130-690-05", "marketing_start_date": "20230613"}], "brand_name": "Naproxen Sodium", "product_id": "21130-690_fe75f23c-9c5e-03a4-e053-6294a90a696d", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-690", "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": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20230613", "listing_expiration_date": "20261231"}