tri-buffered aspirin

Generic: aspirin

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tri-buffered aspirin
Generic Name aspirin
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

aspirin 325 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-517
Product ID 71205-517_ccda47aa-2aeb-4e29-b140-bb903d516bbf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1990-03-30

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 71205517
Hyphenated Format 71205-517

Supplemental Identifiers

RxCUI
212033
UPC
0371205517304
UNII
R16CO5Y76E
NUI
N0000000160 N0000008836 M0001335 N0000175722 N0000175578 N0000008832

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 tri-buffered aspirin (source: ndc)
Generic Name aspirin (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-90)
source: ndc

Packages (3)

71205-517-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-30) 71205-517-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-60) 71205-517-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-90)

Ingredients (1)

aspirin (325 mg/1)

Linked Drug Pages (1)

Tri-Buffered Aspirin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ccda47aa-2aeb-4e29-b140-bb903d516bbf", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "upc": ["0371205517304"], "unii": ["R16CO5Y76E"], "rxcui": ["212033"], "spl_set_id": ["640c3311-2abf-40b2-82b9-9fe4d8c1cf1d"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-30)", "package_ndc": "71205-517-30", "marketing_start_date": "20201230"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-60)", "package_ndc": "71205-517-60", "marketing_start_date": "20201230"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-90)", "package_ndc": "71205-517-90", "marketing_start_date": "20201230"}], "brand_name": "Tri-Buffered Aspirin", "product_id": "71205-517_ccda47aa-2aeb-4e29-b140-bb903d516bbf", "dosage_form": "TABLET, FILM COATED", "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": "71205-517", "generic_name": "Aspirin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tri-Buffered Aspirin", "active_ingredients": [{"name": "ASPIRIN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19900330", "listing_expiration_date": "20261231"}