arthritis pain reliever extended release

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name arthritis pain reliever extended release
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 59726-013
Product ID 59726-013_215e2e69-2d92-4cb7-9f64-a06bcfa7f6e3
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Marketing Start 2020-04-30
Marketing End 2026-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59726013
Hyphenated Format 59726-013

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 arthritis pain reliever extended release (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA211544 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-013-10) / 100 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "215e2e69-2d92-4cb7-9f64-a06bcfa7f6e3", "openfda": {"upc": ["0359726013109"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["0dcf54e7-de0c-426a-9b49-2ac2e8b6bdb0"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-013-10)  / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-013-10", "marketing_end_date": "20260430", "marketing_start_date": "20200430"}], "brand_name": "Arthritis Pain Reliever Extended Release", "product_id": "59726-013_215e2e69-2d92-4cb7-9f64-a06bcfa7f6e3", "dosage_form": "TABLET", "product_ndc": "59726-013", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arthritis Pain Reliever", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20200430"}