naproxen sodium

Generic: naproxen sodium

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler h e b
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-713
Product ID 37808-713_6ee71bc8-3819-4e08-85f5-9557df90ad5a
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 2017-10-03

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 37808713
Hyphenated Format 37808-713

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 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
  • 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)
source: ndc

Packages (1)

37808-713-79 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)

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": "6ee71bc8-3819-4e08-85f5-9557df90ad5a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["b5dcf3df-2628-49c7-9d96-64886bebe631"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)", "package_ndc": "37808-713-79", "marketing_start_date": "20171003"}], "brand_name": "naproxen sodium", "product_id": "37808-713_6ee71bc8-3819-4e08-85f5-9557df90ad5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-713", "generic_name": "Naproxen Sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20171003", "listing_expiration_date": "20261231"}