arthritis pain reliever extended release
Generic: acetaminophen
Labeler: p & l development, llcDrug Facts
Product Profile
Brand Name
arthritis pain reliever extended release
Generic Name
acetaminophen
Labeler
p & l development, llc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 650 mg/1
Manufacturer
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
UPC
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
arthritis pain reliever extended release (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
ANDA211544 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 BOX (59726-013-10) / 100 TABLET in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (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"}