pain reliever

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name pain reliever
Generic Name acetaminophen
Labeler p & l development, llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 49580-2880
Product ID 49580-2880_7dfcadc9-97a1-4d12-b8d9-2053c4ee9273
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2024-03-15
Marketing End 2026-12-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 495802880
Hyphenated Format 49580-2880

Supplemental Identifiers

RxCUI
307668
UPC
0349580288058
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 reliever (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (49580-2880-4) / 118 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

49580-2880-4 1 BOTTLE, PLASTIC in 1 BOX (49580-2880-4) / 118 mL in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

Pain Reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7dfcadc9-97a1-4d12-b8d9-2053c4ee9273", "openfda": {"upc": ["0349580288058"], "unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["64c642b7-ef83-44b7-a014-6fa248dff3ba"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (49580-2880-4)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "49580-2880-4", "marketing_end_date": "20261230", "marketing_start_date": "20240315"}], "brand_name": "Pain Reliever", "product_id": "49580-2880_7dfcadc9-97a1-4d12-b8d9-2053c4ee9273", "dosage_form": "SUSPENSION", "product_ndc": "49580-2880", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261230", "marketing_start_date": "20240315"}