topcare pain relief

Generic: acetaminophen

Labeler: topco associates llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name topcare pain relief
Generic Name acetaminophen
Labeler topco associates llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Topco Associates LLC

Identifiers & Regulatory

Product NDC 36800-484
Product ID 36800-484_5a603472-0c63-455e-b8a0-53761d1bbdcd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1987-07-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 36800484
Hyphenated Format 36800-484

Supplemental Identifiers

RxCUI
198440
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 topcare pain relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 150 TABLET in 1 BOTTLE (36800-484-47)
  • 1 BOTTLE in 1 CARTON (36800-484-62) / 24 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (36800-484-71) / 50 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (36800-484-76) / 120 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (36800-484-78) / 100 TABLET in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (36800-484-82) / 100 TABLET in 1 BOTTLE
  • 500 TABLET in 1 BOTTLE (36800-484-90)
source: ndc

Packages (7)

36800-484-47 150 TABLET in 1 BOTTLE (36800-484-47) 36800-484-62 1 BOTTLE in 1 CARTON (36800-484-62) / 24 TABLET in 1 BOTTLE 36800-484-71 1 BOTTLE in 1 CARTON (36800-484-71) / 50 TABLET in 1 BOTTLE 36800-484-76 1 BOTTLE in 1 CARTON (36800-484-76) / 120 TABLET in 1 BOTTLE 36800-484-78 1 BOTTLE in 1 CARTON (36800-484-78) / 100 TABLET in 1 BOTTLE 36800-484-82 2 BOTTLE in 1 CARTON (36800-484-82) / 100 TABLET in 1 BOTTLE 36800-484-90 500 TABLET in 1 BOTTLE (36800-484-90)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Topcare Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5a603472-0c63-455e-b8a0-53761d1bbdcd", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["6036c15b-1168-4103-9471-6a74a2140e53"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET in 1 BOTTLE (36800-484-47)", "package_ndc": "36800-484-47", "marketing_start_date": "19870715"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-484-62)  / 24 TABLET in 1 BOTTLE", "package_ndc": "36800-484-62", "marketing_start_date": "19870715"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-484-71)  / 50 TABLET in 1 BOTTLE", "package_ndc": "36800-484-71", "marketing_start_date": "19870715"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-484-76)  / 120 TABLET in 1 BOTTLE", "package_ndc": "36800-484-76", "marketing_start_date": "19870715"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-484-78)  / 100 TABLET in 1 BOTTLE", "package_ndc": "36800-484-78", "marketing_start_date": "19870715"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (36800-484-82)  / 100 TABLET in 1 BOTTLE", "package_ndc": "36800-484-82", "marketing_start_date": "19870715"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (36800-484-90)", "package_ndc": "36800-484-90", "marketing_start_date": "19870715"}], "brand_name": "Topcare Pain Relief", "product_id": "36800-484_5a603472-0c63-455e-b8a0-53761d1bbdcd", "dosage_form": "TABLET", "product_ndc": "36800-484", "generic_name": "Acetaminophen", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Topcare Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19870715", "listing_expiration_date": "20261231"}