Adult Low Dose Aspirin

Product NDC: 72789-039
Requested package NDC: 72789-039-35
11-digit product format: 727890039
Labeler code: 72789
Product ID: 72789-039_e60f027d-da80-ec74-e053-2995a90aedb3
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: PD-Rx Pharmaceuticals, Inc.
Application: part343
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2007-01-12
Marketing end: 0000-00-00
Substance: ASPIRIN
Active strength: 81 mg/1
Pharmacologic classes: 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]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	72789-039	72789-039-35	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	72789-039	72789-039-35	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	72789-039	72789-039-35	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72789-039-01	EA - Each	72789-039	f3debe2f-0187-4410-8d9d-c2f5c60e0c16	1	2020-07-13
72789-039-35	EA - Each	72789-039	3a530308-daaf-45fe-8abc-3c56c7fdf11f	1	2020-07-13
72789-039-98	EA - Each	72789-039	858abecd-3d27-43c9-a262-630bb2eb6e35	1	2020-03-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72789-039	ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	9	Legacy NDC	20241010_7d0515c9-666a-4457-97b7-28eb27e25299.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
R16CO5Y76E	ASPIRIN	50-78-2	ASPIRIN

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
72789-039-35	72789003935	35 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-039-35)	2020-05-21	0000-00-00	No	No	Current