acetaminophen

Generic: acetaminophen

Labeler: chain drug marketing association inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler chain drug marketing association inc.
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/15mL

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC.

Identifiers & Regulatory

Product NDC 63868-809
Product ID 63868-809_14e59795-60fb-4d85-baf8-176539f86505
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2023-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868809
Hyphenated Format 63868-809

Supplemental Identifiers

RxCUI
307684
UPC
0635515997646
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

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 M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE (63868-809-08)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (500 mg/15mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14e59795-60fb-4d85-baf8-176539f86505", "openfda": {"upc": ["0635515997646"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["1608b4f0-bf20-4024-b8f2-20a4df7a4b21"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (63868-809-08)", "package_ndc": "63868-809-08", "marketing_start_date": "20230701"}], "brand_name": "Acetaminophen", "product_id": "63868-809_14e59795-60fb-4d85-baf8-176539f86505", "dosage_form": "SYRUP", "product_ndc": "63868-809", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230701", "listing_expiration_date": "20261231"}