naproxen sodium (71335-1925)

Drug Facts

Product Profile

Brand Name naproxen sodium

Generic Name naproxen sodium

Labeler bryant ranch prepack

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

naproxen sodium 275 mg/1

Manufacturer

Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1925

Product ID 71335-1925_5106647a-1c82-4ebe-95f3-db46fb2398db

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA200629

Listing Expiration 2027-12-31

Marketing Start 2011-10-31

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 713351925

Hyphenated Format 71335-1925

Supplemental Identifiers

RxCUI

849398

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 ANDA200629 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

275 mg/1

source: ndc

Packaging

60 TABLET, FILM COATED in 1 BOTTLE (71335-1925-1)
90 TABLET, FILM COATED in 1 BOTTLE (71335-1925-2)
42 TABLET, FILM COATED in 1 BOTTLE (71335-1925-3)
20 TABLET, FILM COATED in 1 BOTTLE (71335-1925-4)
120 TABLET, FILM COATED in 1 BOTTLE (71335-1925-5)
30 TABLET, FILM COATED in 1 BOTTLE (71335-1925-6)

source: ndc

Packages (6)

71335-1925-1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1925-1) 71335-1925-2 90 TABLET, FILM COATED in 1 BOTTLE (71335-1925-2) 71335-1925-3 42 TABLET, FILM COATED in 1 BOTTLE (71335-1925-3) 71335-1925-4 20 TABLET, FILM COATED in 1 BOTTLE (71335-1925-4) 71335-1925-5 120 TABLET, FILM COATED in 1 BOTTLE (71335-1925-5) 71335-1925-6 30 TABLET, FILM COATED in 1 BOTTLE (71335-1925-6)

Ingredients (1)

naproxen sodium (275 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": "5106647a-1c82-4ebe-95f3-db46fb2398db", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849398"], "spl_set_id": ["1c2325f7-1d65-429d-a64d-6ab075df1c20"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1925-1)", "package_ndc": "71335-1925-1", "marketing_start_date": "20250130"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1925-2)", "package_ndc": "71335-1925-2", "marketing_start_date": "20250130"}, {"sample": false, "description": "42 TABLET, FILM COATED in 1 BOTTLE (71335-1925-3)", "package_ndc": "71335-1925-3", "marketing_start_date": "20250130"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1925-4)", "package_ndc": "71335-1925-4", "marketing_start_date": "20250130"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1925-5)", "package_ndc": "71335-1925-5", "marketing_start_date": "20250130"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1925-6)", "package_ndc": "71335-1925-6", "marketing_start_date": "20210729"}], "brand_name": "Naproxen Sodium", "product_id": "71335-1925_5106647a-1c82-4ebe-95f3-db46fb2398db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-1925", "generic_name": "Naproxen Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "275 mg/1"}], "application_number": "ANDA200629", "marketing_category": "ANDA", "marketing_start_date": "20111031", "listing_expiration_date": "20271231"}