naproxen

Generic: naproxen

Labeler: safeway, inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen
Labeler safeway, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Safeway, Inc

Identifiers & Regulatory

Product NDC 21130-062
Product ID 21130-062_4650a28b-d299-a5e5-e063-6294a90ad9f7
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091353
Listing Expiration 2026-12-31
Marketing Start 2023-08-30

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 21130062
Hyphenated Format 21130-062

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 (source: ndc)
Generic Name naproxen (source: ndc)
Application Number ANDA091353 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 50 TABLET in 1 BOTTLE (21130-062-05)
  • 90 TABLET in 1 BOTTLE (21130-062-09)
  • 200 TABLET in 1 BOTTLE (21130-062-20)
source: ndc

Packages (3)

21130-062-05 50 TABLET in 1 BOTTLE (21130-062-05) 21130-062-09 90 TABLET in 1 BOTTLE (21130-062-09) 21130-062-20 200 TABLET in 1 BOTTLE (21130-062-20)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Naproxen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4650a28b-d299-a5e5-e063-6294a90ad9f7", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f2a273f8-d623-dc2f-e053-2995a90a0c02"], "manufacturer_name": ["Safeway, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (21130-062-05)", "package_ndc": "21130-062-05", "marketing_start_date": "20230830"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (21130-062-09)", "package_ndc": "21130-062-09", "marketing_start_date": "20230830"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (21130-062-20)", "package_ndc": "21130-062-20", "marketing_start_date": "20230930"}], "brand_name": "Naproxen", "product_id": "21130-062_4650a28b-d299-a5e5-e063-6294a90ad9f7", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-062", "generic_name": "Naproxen", "labeler_name": "Safeway, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20230830", "listing_expiration_date": "20261231"}