acetaminophen pain reliever fever reducer

Generic: acetaminophen

Labeler: padagis israel pharmaceuticals ltd
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen pain reliever fever reducer
Generic Name acetaminophen
Labeler padagis israel pharmaceuticals ltd
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Padagis Israel Pharmaceuticals Ltd

Identifiers & Regulatory

Product NDC 45802-730
Product ID 45802-730_4926c350-ee6f-446c-a63d-cc7170f9a68c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA070608
Marketing Start 2010-10-28
Marketing End 2026-11-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 45802730
Hyphenated Format 45802-730

Supplemental Identifiers

RxCUI
198443
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 pain reliever fever reducer (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA070608 (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 SUPPOSITORY in 1 BLISTER PACK (45802-730-00)
  • 12 BLISTER PACK in 1 CARTON (45802-730-30) / 1 SUPPOSITORY in 1 BLISTER PACK
  • 50 BLISTER PACK in 1 CARTON (45802-730-32) / 1 SUPPOSITORY in 1 BLISTER PACK
  • 100 BLISTER PACK in 1 CARTON (45802-730-33) / 1 SUPPOSITORY in 1 BLISTER PACK
source: ndc

Packages (4)

45802-730-00 1 SUPPOSITORY in 1 BLISTER PACK (45802-730-00) 45802-730-30 12 BLISTER PACK in 1 CARTON (45802-730-30) / 1 SUPPOSITORY in 1 BLISTER PACK 45802-730-32 50 BLISTER PACK in 1 CARTON (45802-730-32) / 1 SUPPOSITORY in 1 BLISTER PACK 45802-730-33 100 BLISTER PACK in 1 CARTON (45802-730-33) / 1 SUPPOSITORY in 1 BLISTER PACK

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

acetaminophen pain reliever fever reducer ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RECTAL"], "spl_id": "4926c350-ee6f-446c-a63d-cc7170f9a68c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198443"], "spl_set_id": ["b43974c3-4db9-4201-beee-b22596a2b241"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SUPPOSITORY in 1 BLISTER PACK (45802-730-00)", "package_ndc": "45802-730-00", "marketing_end_date": "20261130", "marketing_start_date": "20101028"}, {"sample": false, "description": "12 BLISTER PACK in 1 CARTON (45802-730-30)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "45802-730-30", "marketing_end_date": "20261130", "marketing_start_date": "20101028"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (45802-730-32)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "45802-730-32", "marketing_end_date": "20261130", "marketing_start_date": "20101122"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (45802-730-33)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "45802-730-33", "marketing_end_date": "20261130", "marketing_start_date": "20101028"}], "brand_name": "acetaminophen pain reliever fever reducer", "product_id": "45802-730_4926c350-ee6f-446c-a63d-cc7170f9a68c", "dosage_form": "SUPPOSITORY", "product_ndc": "45802-730", "generic_name": "Acetaminophen", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "acetaminophen", "brand_name_suffix": "pain reliever fever reducer", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA070608", "marketing_category": "ANDA", "marketing_end_date": "20261130", "marketing_start_date": "20101028"}