regular strength pain relief
Generic: acetaminophen
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
regular strength pain relief
Generic Name
acetaminophen
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2252
Product ID
72162-2252_2ab345c2-b547-480a-b88c-7dbda6432ef9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
1989-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622252
Hyphenated Format
72162-2252
Supplemental Identifiers
RxCUI
UNII
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
regular strength pain relief (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (72162-2252-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ab345c2-b547-480a-b88c-7dbda6432ef9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["3f0c32b1-2c54-4ca3-9759-9e5dd9d7ad24"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2252-1)", "package_ndc": "72162-2252-1", "marketing_start_date": "20111201"}], "brand_name": "Regular Strength Pain Relief", "product_id": "72162-2252_2ab345c2-b547-480a-b88c-7dbda6432ef9", "dosage_form": "TABLET", "product_ndc": "72162-2252", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Regular Strength Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19890101", "listing_expiration_date": "20261231"}