basic care naproxen sodium

Generic: naproxen sodium

Labeler: amazon.com services llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name basic care naproxen sodium
Generic Name naproxen sodium
Labeler amazon.com services llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Amazon.com Services LLC

Identifiers & Regulatory

Product NDC 72288-368
Product ID 72288-368_a6153243-3d4b-4a22-9799-521a40f37be1
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 2020-05-18

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 72288368
Hyphenated Format 72288-368

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 basic care 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
  • 1 BOTTLE in 1 CARTON (72288-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (72288-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE
  • 300 TABLET, FILM COATED in 1 BOTTLE (72288-368-87)
source: ndc

Packages (3)

72288-368-75 1 BOTTLE in 1 CARTON (72288-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE 72288-368-82 1 BOTTLE in 1 CARTON (72288-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE 72288-368-87 300 TABLET, FILM COATED in 1 BOTTLE (72288-368-87)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

basic care naproxen sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6153243-3d4b-4a22-9799-521a40f37be1", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["29fc5a16-49ed-41ca-a296-bee34d1d12f6"], "manufacturer_name": ["Amazon.com Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72288-368-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "72288-368-75", "marketing_start_date": "20230116"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (72288-368-82)  / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "72288-368-82", "marketing_start_date": "20200521"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (72288-368-87)", "package_ndc": "72288-368-87", "marketing_start_date": "20200518"}], "brand_name": "basic care naproxen sodium", "product_id": "72288-368_a6153243-3d4b-4a22-9799-521a40f37be1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72288-368", "generic_name": "Naproxen Sodium", "labeler_name": "Amazon.com Services LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "basic care naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20200518", "listing_expiration_date": "20261231"}