naproxen sodium headache pain
Generic: naproxen sodium
Labeler: aurohealth llcDrug Facts
Product Profile
Brand Name
naproxen sodium headache pain
Generic Name
naproxen sodium
Labeler
aurohealth llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58602-735
Product ID
58602-735_b14dd7e8-b43c-4d9e-9609-13d9f30a74c4
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA205497
Listing Expiration
2026-12-31
Marketing Start
2021-07-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58602735
Hyphenated Format
58602-735
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
naproxen sodium headache pain (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
ANDA205497 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (58602-735-07) / 24 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-735-19) / 90 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-735-21) / 100 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-735-29) / 150 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-735-38) / 300 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-735-40) / 500 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (58602-735-78) / 50 TABLET, FILM COATED in 1 BOTTLE
Packages (7)
58602-735-07
1 BOTTLE in 1 CARTON (58602-735-07) / 24 TABLET, FILM COATED in 1 BOTTLE
58602-735-19
1 BOTTLE in 1 CARTON (58602-735-19) / 90 TABLET, FILM COATED in 1 BOTTLE
58602-735-21
1 BOTTLE in 1 CARTON (58602-735-21) / 100 TABLET, FILM COATED in 1 BOTTLE
58602-735-29
1 BOTTLE in 1 CARTON (58602-735-29) / 150 TABLET, FILM COATED in 1 BOTTLE
58602-735-38
1 BOTTLE in 1 CARTON (58602-735-38) / 300 TABLET, FILM COATED in 1 BOTTLE
58602-735-40
1 BOTTLE in 1 CARTON (58602-735-40) / 500 TABLET, FILM COATED in 1 BOTTLE
58602-735-78
1 BOTTLE in 1 CARTON (58602-735-78) / 50 TABLET, FILM COATED in 1 BOTTLE
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b14dd7e8-b43c-4d9e-9609-13d9f30a74c4", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["e4a9ea0e-aec4-493c-b9b4-5e5a91d260d5"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-735-07) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-735-07", "marketing_start_date": "20210714"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-735-19) / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-735-19", "marketing_start_date": "20230921"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-735-21) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-735-21", "marketing_start_date": "20210714"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-735-29) / 150 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-735-29", "marketing_start_date": "20210714"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-735-38) / 300 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-735-38", "marketing_start_date": "20210714"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-735-40) / 500 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-735-40", "marketing_start_date": "20210714"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-735-78) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-735-78", "marketing_start_date": "20210714"}], "brand_name": "Naproxen Sodium HEADACHE PAIN", "product_id": "58602-735_b14dd7e8-b43c-4d9e-9609-13d9f30a74c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "58602-735", "generic_name": "Naproxen Sodium", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium HEADACHE PAIN", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA205497", "marketing_category": "ANDA", "marketing_start_date": "20210714", "listing_expiration_date": "20261231"}