extra strength pain relief

Generic: acetaminophen

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength pain relief
Generic Name acetaminophen
Labeler preferred pharmaceuticals inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/15mL

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8375
Product ID 68788-8375_7ba209ec-3695-4163-8ca0-61c894fad3bf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 343
Listing Expiration 2026-12-31
Marketing Start 2023-02-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888375
Hyphenated Format 68788-8375

Supplemental Identifiers

UNII
362O9ITL9D

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 extra strength pain relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number 343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE (68788-8375-2)
source: ndc

Packages (1)

68788-8375-2 237 mL in 1 BOTTLE (68788-8375-2)

Ingredients (1)

acetaminophen (500 mg/15mL)

Linked Drug Pages (1)

EXTRA STRENGTH PAIN RELIEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7ba209ec-3695-4163-8ca0-61c894fad3bf", "openfda": {"unii": ["362O9ITL9D"], "spl_set_id": ["e18294f5-8fd5-4ac6-802c-f6d257e8bee7"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (68788-8375-2)", "package_ndc": "68788-8375-2", "marketing_start_date": "20230224"}], "brand_name": "EXTRA STRENGTH PAIN RELIEF", "product_id": "68788-8375_7ba209ec-3695-4163-8ca0-61c894fad3bf", "dosage_form": "SUSPENSION", "product_ndc": "68788-8375", "generic_name": "Acetaminophen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH PAIN RELIEF", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "343", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230224", "listing_expiration_date": "20261231"}