aspirin pain reliver

Generic: aspirin

Labeler: pioneer life sciences, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name aspirin pain reliver
Generic Name aspirin
Labeler pioneer life sciences, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aspirin 81 mg/1

Manufacturer
Pioneer Life Sciences, LLC

Identifiers & Regulatory

Product NDC 72090-034
Product ID 72090-034_ee1c0ed7-e39d-4d8b-b7b8-fb10ce496321
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-09-12

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc] platelet aggregation inhibitor [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]
Physiologic Effect
decreased prostaglandin production [pe] decreased platelet aggregation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72090034
Hyphenated Format 72090-034

Supplemental Identifiers

RxCUI
308416
UPC
0372090002937
UNII
R16CO5Y76E
NUI
N0000000160 N0000008836 M0001335 N0000175722 N0000175578 N0000008832

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 aspirin pain reliver (source: ndc)
Generic Name aspirin (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 81 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (72090-034-01)
  • 1000 TABLET in 1 BOTTLE (72090-034-02)
source: ndc

Packages (2)

Ingredients (1)

aspirin (81 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee1c0ed7-e39d-4d8b-b7b8-fb10ce496321", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "upc": ["0372090002937"], "unii": ["R16CO5Y76E"], "rxcui": ["308416"], "spl_set_id": ["8dc29957-2ac1-47f8-89fd-a6bcf97ee3d3"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_pe": ["Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72090-034-01)", "package_ndc": "72090-034-01", "marketing_start_date": "20240912"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72090-034-02)", "package_ndc": "72090-034-02", "marketing_start_date": "20240912"}], "brand_name": "Aspirin Pain reliver", "product_id": "72090-034_ee1c0ed7-e39d-4d8b-b7b8-fb10ce496321", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "product_ndc": "72090-034", "generic_name": "Aspirin", "labeler_name": "Pioneer Life Sciences, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aspirin Pain reliver", "active_ingredients": [{"name": "ASPIRIN", "strength": "81 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240912", "listing_expiration_date": "20261231"}