naproxen sodium

Generic: naproxen sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 550 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5238
Product ID 50090-5238_a4e99a96-8609-4a3c-987a-42be7d2e1dab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078486
Listing Expiration 2027-12-31
Marketing Start 2016-04-26

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 500905238
Hyphenated Format 50090-5238

Supplemental Identifiers

RxCUI
849431
UNII
9TN87S3A3C

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 (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA078486 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 550 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-5238-3)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-5238-5)
source: ndc

Packages (2)

50090-5238-3 20 TABLET, FILM COATED in 1 BOTTLE (50090-5238-3) 50090-5238-5 30 TABLET, FILM COATED in 1 BOTTLE (50090-5238-5)

Ingredients (1)

naproxen sodium (550 mg/1)

Linked Drug Pages (1)

Naproxen sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a4e99a96-8609-4a3c-987a-42be7d2e1dab", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["8181bb7a-d917-4388-bcb0-a74671b07b06"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-5238-3)", "package_ndc": "50090-5238-3", "marketing_start_date": "20201009"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5238-5)", "package_ndc": "50090-5238-5", "marketing_start_date": "20201009"}], "brand_name": "Naproxen sodium", "product_id": "50090-5238_a4e99a96-8609-4a3c-987a-42be7d2e1dab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-5238", "generic_name": "Naproxen sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "550 mg/1"}], "application_number": "ANDA078486", "marketing_category": "ANDA", "marketing_start_date": "20160426", "listing_expiration_date": "20271231"}