careone naproxen sodium

Generic: naproxen sodium

Labeler: american sales company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name careone naproxen sodium
Generic Name naproxen sodium
Labeler american sales company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
American Sales Company

Identifiers & Regulatory

Product NDC 41520-507
Product ID 41520-507_b1921833-7307-4f20-84bb-d63dab25a76c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 2016-08-05

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 41520507
Hyphenated Format 41520-507

Supplemental Identifiers

RxCUI
849574
UNII
9TN87S3A3C

Packaging Origin

Original Packager
true

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 careone naproxen sodium (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA074661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (41520-507-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (41520-507-75) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 300 TABLET, FILM COATED in 1 BOTTLE (41520-507-87)
source: ndc

Packages (3)

41520-507-71 1 BOTTLE in 1 CARTON (41520-507-71) / 50 TABLET, FILM COATED in 1 BOTTLE 41520-507-75 1 BOTTLE in 1 CARTON (41520-507-75) / 90 TABLET, FILM COATED in 1 BOTTLE 41520-507-87 300 TABLET, FILM COATED in 1 BOTTLE (41520-507-87)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

CareOne Naproxen Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b1921833-7307-4f20-84bb-d63dab25a76c", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["0ac4c343-a5b6-4f69-a75a-87074dc867e8"], "manufacturer_name": ["American Sales Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41520-507-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41520-507-71", "marketing_start_date": "20160805"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41520-507-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41520-507-75", "marketing_start_date": "20220225"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (41520-507-87)", "package_ndc": "41520-507-87", "marketing_start_date": "20180525"}], "brand_name": "CareOne Naproxen Sodium", "product_id": "41520-507_b1921833-7307-4f20-84bb-d63dab25a76c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41520-507", "generic_name": "Naproxen Sodium", "labeler_name": "American Sales Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CareOne Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20160805", "listing_expiration_date": "20261231"}