pain relief extra strength

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name pain relief extra strength
Generic Name acetaminophen
Labeler l.n.k. international, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
L.N.K. International, Inc.

Identifiers & Regulatory

Product NDC 50844-951
Product ID 50844-951_30ddbaa9-9ef6-41d9-b257-ae3003113729
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2004-05-10
Marketing End 2026-05-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50844951
Hyphenated Format 50844-951

Supplemental Identifiers

UPC
0350844951205
UNII
362O9ITL9D

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 pain relief extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-951-15) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-951-20)
source: ndc

Packages (2)

50844-951-15 1 BOTTLE, PLASTIC in 1 CARTON (50844-951-15) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 50844-951-20 225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-951-20)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "30ddbaa9-9ef6-41d9-b257-ae3003113729", "openfda": {"upc": ["0350844951205"], "unii": ["362O9ITL9D"], "spl_set_id": ["09c9a9d9-f14e-4343-9677-188f20d4d148"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-951-15)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-951-15", "marketing_end_date": "20260531", "marketing_start_date": "20040510"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-951-20)", "package_ndc": "50844-951-20", "marketing_end_date": "20260531", "marketing_start_date": "20040510"}], "brand_name": "Pain Relief Extra Strength", "product_id": "50844-951_30ddbaa9-9ef6-41d9-b257-ae3003113729", "dosage_form": "TABLET, COATED", "product_ndc": "50844-951", "generic_name": "Acetaminophen", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260531", "marketing_start_date": "20040510"}