pain reliever extra strength

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 extra strength
Generic Name acetaminophen
Labeler p & l development, llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/15mL

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 49580-3278
Product ID 49580-3278_5a915cb3-5df8-4967-9290-b1dc797ec257
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2019-11-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 495803278
Hyphenated Format 49580-3278

Supplemental Identifiers

RxCUI
307684
UPC
0349580278080
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 extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE, PLASTIC (49580-3278-8)
source: ndc

Packages (1)

49580-3278-8 237 mL in 1 BOTTLE, PLASTIC (49580-3278-8)

Ingredients (1)

acetaminophen (500 mg/15mL)

Linked Drug Pages (1)

Pain Reliever Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5a915cb3-5df8-4967-9290-b1dc797ec257", "openfda": {"upc": ["0349580278080"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["061df1fd-173a-4bd1-9600-540ac0f3964d"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (49580-3278-8)", "package_ndc": "49580-3278-8", "marketing_start_date": "20191129"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "49580-3278_5a915cb3-5df8-4967-9290-b1dc797ec257", "dosage_form": "LIQUID", "product_ndc": "49580-3278", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191129", "listing_expiration_date": "20261231"}