aspirin regimen

Generic: aspirin

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name aspirin regimen
Generic Name aspirin
Labeler cardinal health 110, llc. dba leader
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

aspirin 81 mg/1

Manufacturer
Cardinal Health 110, LLC. DBA Leader

Identifiers & Regulatory

Product NDC 70000-0603
Product ID 70000-0603_ac98a2c6-4823-49a7-a281-deb171a56701
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-05-05

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 700000603
Hyphenated Format 70000-0603

Supplemental Identifiers

RxCUI
308416
UPC
0096295142006
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 regimen (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
  • 1 BOTTLE, PLASTIC in 1 CARTON (70000-0603-1) / 32 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (70000-0603-2) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
  • 300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70000-0603-3)
source: ndc

Packages (3)

Ingredients (1)

aspirin (81 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ac98a2c6-4823-49a7-a281-deb171a56701", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "upc": ["0096295142006"], "unii": ["R16CO5Y76E"], "rxcui": ["308416"], "spl_set_id": ["ef2d75ee-9ed7-4b53-adbc-2ec40364da63"], "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": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70000-0603-1)  / 32 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "70000-0603-1", "marketing_start_date": "20220505"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70000-0603-2)  / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "70000-0603-2", "marketing_start_date": "20220505"}, {"sample": false, "description": "300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70000-0603-3)", "package_ndc": "70000-0603-3", "marketing_start_date": "20220505"}], "brand_name": "Aspirin Regimen", "product_id": "70000-0603_ac98a2c6-4823-49a7-a281-deb171a56701", "dosage_form": "TABLET, DELAYED RELEASE", "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": "70000-0603", "generic_name": "Aspirin", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aspirin Regimen", "active_ingredients": [{"name": "ASPIRIN", "strength": "81 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220505", "listing_expiration_date": "20261231"}