Package 43598-058-29

Brand: naproxen sodium caplets

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 43598-058-29
Digits Only 4359805829
Product NDC 43598-058
Description

200 TABLET, COATED in 1 BOTTLE (43598-058-29)

Marketing

Marketing Status
Marketed Since 2021-08-04
Brand naproxen sodium caplets
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c8d85dc-7bf0-a540-f37f-d1f91ff908f9", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["ee0463bc-e939-1ecf-5a86-d045c426fecf"], "manufacturer_name": ["Dr Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, COATED in 1 BOTTLE (43598-058-29)", "package_ndc": "43598-058-29", "marketing_start_date": "20210804"}], "brand_name": "Naproxen Sodium Caplets", "product_id": "43598-058_4c8d85dc-7bf0-a540-f37f-d1f91ff908f9", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43598-058", "generic_name": "Naproxen Sodium", "labeler_name": "Dr Reddy's Laboratories Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "brand_name_suffix": "Caplets", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA075168", "marketing_category": "ANDA", "marketing_start_date": "20210804", "listing_expiration_date": "20261231"}