naproxen sodium

Generic: naproxen sodium

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

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler safeway, inc.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Safeway, Inc.

Identifiers & Regulatory

Product NDC 21130-748
Product ID 21130-748_5e01ba5d-f779-49d2-a5cb-8220991f67a5
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA208363
Marketing Start 2018-04-01
Marketing End 2027-04-01

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 21130748
Hyphenated Format 21130-748

Supplemental Identifiers

RxCUI
1112231
UPC
0321130798538
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 ANDA208363 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (21130-748-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 BOX (21130-748-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (21130-748-80)
source: ndc

Packages (3)

21130-748-20 1 BOTTLE, PLASTIC in 1 BOX (21130-748-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC 21130-748-40 1 BOTTLE, PLASTIC in 1 BOX (21130-748-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC 21130-748-80 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (21130-748-80)

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": "5e01ba5d-f779-49d2-a5cb-8220991f67a5", "openfda": {"upc": ["0321130798538"], "unii": ["9TN87S3A3C"], "rxcui": ["1112231"], "spl_set_id": ["deb1be0f-64ae-46b5-b54a-1a58eec6492e"], "manufacturer_name": ["Safeway, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-748-20)  / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-748-20", "marketing_end_date": "20270401", "marketing_start_date": "20180401"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (21130-748-40)  / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-748-40", "marketing_end_date": "20270401", "marketing_start_date": "20180401"}, {"sample": false, "description": "80 CAPSULE, LIQUID FILLED in 1 BOTTLE (21130-748-80)", "package_ndc": "21130-748-80", "marketing_end_date": "20270401", "marketing_start_date": "20180401"}], "brand_name": "Naproxen Sodium", "product_id": "21130-748_5e01ba5d-f779-49d2-a5cb-8220991f67a5", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-748", "generic_name": "Naproxen Sodium", "labeler_name": "Safeway, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA208363", "marketing_category": "ANDA", "marketing_end_date": "20270401", "marketing_start_date": "20180401"}