arthritispain relief

Generic: acetaminophen

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arthritispain relief
Generic Name acetaminophen
Labeler p & l development, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-669
Product ID 59726-669_9a10f457-df6b-450b-aab3-738b23e0faf6
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207035
Marketing Start 2021-04-30
Marketing End 2026-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59726669
Hyphenated Format 59726-669

Supplemental Identifiers

RxCUI
1148399
UPC
0359726013109
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 arthritispain relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA207035 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-669-10) / 100 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

59726-669-10 1 BOTTLE, PLASTIC in 1 BOX (59726-669-10) / 100 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

ArthritisPain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9a10f457-df6b-450b-aab3-738b23e0faf6", "openfda": {"upc": ["0359726013109"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["4d27405b-a384-43a0-af15-43378d30b9f4"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-669-10)  / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-669-10", "marketing_end_date": "20260430", "marketing_start_date": "20210430"}], "brand_name": "ArthritisPain Relief", "product_id": "59726-669_9a10f457-df6b-450b-aab3-738b23e0faf6", "dosage_form": "TABLET", "product_ndc": "59726-669", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ArthritisPain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA207035", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20210430"}