naproxen sodium
Generic: naproxen sodium
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
naproxen sodium
Generic Name
naproxen sodium
Labeler
cvs pharmacy
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-811
Product ID
69842-811_318d0736-0227-4daf-90f7-e3b3bc606764
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA074661
Listing Expiration
2027-12-31
Marketing Start
2018-05-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842811
Hyphenated Format
69842-811
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (69842-811-62) / 24 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (69842-811-71) / 50 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (69842-811-75) / 90 TABLET, FILM COATED in 1 BOTTLE
- 500 TABLET, FILM COATED in 1 BOTTLE (69842-811-90)
Packages (4)
69842-811-62
1 BOTTLE in 1 CARTON (69842-811-62) / 24 TABLET, FILM COATED in 1 BOTTLE
69842-811-71
1 BOTTLE in 1 CARTON (69842-811-71) / 50 TABLET, FILM COATED in 1 BOTTLE
69842-811-75
1 BOTTLE in 1 CARTON (69842-811-75) / 90 TABLET, FILM COATED in 1 BOTTLE
69842-811-90
500 TABLET, FILM COATED in 1 BOTTLE (69842-811-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "318d0736-0227-4daf-90f7-e3b3bc606764", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["efe4352f-856b-4ada-8bd4-0a78423447dc"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-811-62) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-811-62", "marketing_start_date": "20180509"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-811-71) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-811-71", "marketing_start_date": "20180509"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-811-75) / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-811-75", "marketing_start_date": "20220408"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69842-811-90)", "package_ndc": "69842-811-90", "marketing_start_date": "20180509"}], "brand_name": "Naproxen Sodium", "product_id": "69842-811_318d0736-0227-4daf-90f7-e3b3bc606764", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69842-811", "generic_name": "Naproxen Sodium", "labeler_name": "CVS Pharmacy", "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": "20180509", "listing_expiration_date": "20271231"}