naproxen sodium

Generic: naproxen sodium

Labeler: bi-mart
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler bi-mart
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Bi-Mart

Identifiers & Regulatory

Product NDC 37835-594
Product ID 37835-594_313c8866-b504-7387-e063-6394a90a197f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091353
Listing Expiration 2026-12-31
Marketing Start 2011-09-30

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 37835594
Hyphenated Format 37835-594

Supplemental Identifiers

RxCUI
849574
UPC
0071357903481
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 naproxen sodium (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA091353 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (37835-594-01)
  • 300 TABLET in 1 BOTTLE (37835-594-03)
source: ndc

Packages (2)

37835-594-01 100 TABLET in 1 BOTTLE (37835-594-01) 37835-594-03 300 TABLET in 1 BOTTLE (37835-594-03)

Ingredients (1)

naproxen sodium (220 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": "313c8866-b504-7387-e063-6394a90a197f", "openfda": {"upc": ["0071357903481"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["6d5cecc9-5095-477b-bfc7-45b6e7e689f0"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37835-594-01)", "package_ndc": "37835-594-01", "marketing_start_date": "20250301"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (37835-594-03)", "package_ndc": "37835-594-03", "marketing_start_date": "20250301"}], "brand_name": "Naproxen Sodium", "product_id": "37835-594_313c8866-b504-7387-e063-6394a90a197f", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37835-594", "generic_name": "Naproxen Sodium", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20110930", "listing_expiration_date": "20261231"}