acetaminophen

Generic: acetaminophen

Labeler: bryant ranch prepack
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1340
Product ID 71335-1340_4534cfd2-5503-42bd-829b-5db07a93ce4b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Listing Expiration 2026-12-31
Marketing Start 2019-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351340
Hyphenated Format 71335-1340

Supplemental Identifiers

RxCUI
1148399
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 acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA211544 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-1)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-2)
  • 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-4)
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-5)
  • 19 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-6)
  • 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-7)
source: ndc

Packages (7)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4534cfd2-5503-42bd-829b-5db07a93ce4b", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["f6dc5576-9ba3-436c-87f5-8d0d6258adef"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-1)", "package_ndc": "71335-1340-1", "marketing_start_date": "20191204"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-2)", "package_ndc": "71335-1340-2", "marketing_start_date": "20190820"}, {"sample": false, "description": "50 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-3)", "package_ndc": "71335-1340-3", "marketing_start_date": "20241007"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-4)", "package_ndc": "71335-1340-4", "marketing_start_date": "20241007"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-5)", "package_ndc": "71335-1340-5", "marketing_start_date": "20240723"}, {"sample": false, "description": "19 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-6)", "package_ndc": "71335-1340-6", "marketing_start_date": "20241007"}, {"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1340-7)", "package_ndc": "71335-1340-7", "marketing_start_date": "20241007"}], "brand_name": "ACETAMINOPHEN", "product_id": "71335-1340_4534cfd2-5503-42bd-829b-5db07a93ce4b", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "71335-1340", "generic_name": "ACETAMINOPHEN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}