pain relief
Generic: acetaminophen
Labeler: meijer distribution incDrug Facts
Product Profile
Brand Name
pain relief
Generic Name
acetaminophen
Labeler
meijer distribution inc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
41250-403
Product ID
41250-403_25e3435c-d64a-4fba-85df-9bec6346e52e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-06-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41250403
Hyphenated Format
41250-403
Supplemental Identifiers
RxCUI
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
pain relief (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (41250-403-78) / 100 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "25e3435c-d64a-4fba-85df-9bec6346e52e", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["43c3fe72-a4ef-48a6-bc22-a644919c0c5c"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-403-78) / 100 TABLET in 1 BOTTLE", "package_ndc": "41250-403-78", "marketing_start_date": "20240617"}], "brand_name": "pain relief", "product_id": "41250-403_25e3435c-d64a-4fba-85df-9bec6346e52e", "dosage_form": "TABLET", "product_ndc": "41250-403", "generic_name": "Acetaminophen", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240617", "listing_expiration_date": "20261231"}