naproxen back and muscle pain

Generic: naproxen sodium

Labeler: l.n.k. international, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen back and muscle pain
Generic Name naproxen sodium
Labeler l.n.k. international, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
L.N.K. International, Inc.

Identifiers & Regulatory

Product NDC 50844-714
Product ID 50844-714_bc397444-6e0e-4b4e-8f03-d6372588d8ab
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204872
Listing Expiration 2027-12-31
Marketing Start 2019-02-01

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 50844714
Hyphenated Format 50844-714

Supplemental Identifiers

RxCUI
849574
UPC
0350844714169
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 back and muscle pain (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA204872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16)
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56)
  • 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98)
  • 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)
source: ndc

Packages (6)

50844-714-14 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14) 50844-714-16 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16) 50844-714-19 1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 50844-714-56 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56) 50844-714-98 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98) 50844-714-99 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Naproxen Back and Muscle Pain ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bc397444-6e0e-4b4e-8f03-d6372588d8ab", "openfda": {"upc": ["0350844714169"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["68944663-0dc0-4d3a-a36b-019061bdbfa0"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)", "package_ndc": "50844-714-14", "marketing_start_date": "20190201"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16)", "package_ndc": "50844-714-16", "marketing_start_date": "20190201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19)  / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-714-19", "marketing_start_date": "20190201"}, {"sample": false, "description": "25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56)", "package_ndc": "50844-714-56", "marketing_start_date": "20190201"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98)", "package_ndc": "50844-714-98", "marketing_start_date": "20190201"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)", "package_ndc": "50844-714-99", "marketing_start_date": "20190201"}], "brand_name": "Naproxen Back and Muscle Pain", "product_id": "50844-714_bc397444-6e0e-4b4e-8f03-d6372588d8ab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50844-714", "generic_name": "Naproxen Sodium", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Back and Muscle Pain", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20190201", "listing_expiration_date": "20271231"}