childrens acetaminophen
Generic: acetaminophen
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
childrens acetaminophen
Generic Name
acetaminophen
Labeler
bryant ranch prepack
Dosage Form
SUSPENSION
Routes
Active Ingredients
acetaminophen 160 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2722
Product ID
71335-2722_e7fdf4db-c5e3-433a-8e94-13f5c25ca933
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2014-04-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352722
Hyphenated Format
71335-2722
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
childrens acetaminophen (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (71335-2722-1) / 118 mL 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": "e7fdf4db-c5e3-433a-8e94-13f5c25ca933", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["190bb2dc-92b4-4b59-a47f-a0251df8261c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71335-2722-1) / 118 mL in 1 BOTTLE", "package_ndc": "71335-2722-1", "marketing_start_date": "20250729"}], "brand_name": "Childrens Acetaminophen", "product_id": "71335-2722_e7fdf4db-c5e3-433a-8e94-13f5c25ca933", "dosage_form": "SUSPENSION", "product_ndc": "71335-2722", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Childrens Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140409", "listing_expiration_date": "20261231"}