acetaminophen
Generic: acetaminophen
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
nucare pharmaceuticals,inc.
Dosage Form
SUSPENSION
Routes
Active Ingredients
acetaminophen 160 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4860
Product ID
68071-4860_1ae1a5f4-8419-25d8-e063-6294a90a35c6
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2026-12-31
Marketing Start
2014-04-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680714860
Hyphenated Format
68071-4860
Supplemental Identifiers
RxCUI
UPC
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
acetaminophen (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/5mL
Packaging
- 118 mL in 1 BOTTLE (68071-4860-4)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ae1a5f4-8419-25d8-e063-6294a90a35c6", "openfda": {"upc": ["0368071486049"], "unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["872365ca-0c6b-550a-e053-2a91aa0ab25a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (68071-4860-4)", "package_ndc": "68071-4860-4", "marketing_start_date": "20190422"}], "brand_name": "Acetaminophen", "product_id": "68071-4860_1ae1a5f4-8419-25d8-e063-6294a90a35c6", "dosage_form": "SUSPENSION", "product_ndc": "68071-4860", "generic_name": "Acetaminophen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140409", "listing_expiration_date": "20261231"}