Aspirin 81 mg

Product NDC: 55910-600
11-digit product format: 559100600
Labeler code: 55910
Product ID: 55910-600_15dd3324-0cca-45d0-8c73-794a6027ae5d
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: DOLGENCORP, LLC
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-05-01
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: 2027-12-31
Current FDA listing: Yes

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	55910-600	55910-600-69	D	Discontinued by firm		2026-10-27

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Aspirin 81 mg
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ASPIRIN	81 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
R16CO5Y76E	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
308416	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
b4064039-2345-4227-b83d-54dc13a838d3	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
d7724692-1155-4cc8-a415-22f5fc4aec35	Product name	6	20220216
bde672ba-4805-28d0-1986-73543d41b412	Product name	2	20210201
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
ade821ba-260a-47e2-bd89-743e27ac9906	Product name	1	20161121
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657	Product name	1	20150929
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
2a21311a-89e2-0e83-2ebd-117f9798b2b2	Product name	1	20140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94e	Product name	1	20140508
96c2be53-8e44-452d-56a2-d255b2f1af2d	Product name	1	20140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55910-600-32	Aspirin 81 mg	120 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	120	24
55910-600-32	Aspirin 81 mg	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	24
55910-600-69	Aspirin 81 mg	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	24
55910-600-69	Aspirin 81 mg	144 in 1 BOTTLE	TABLET, DELAYED RELEASE	144	24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [DOLGENCORP, LLC]	10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55910-600	ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [DOLGENCORP, LLC]	22	Current NDC, Legacy NDC, 4 package rows	20240825_b4064039-2345-4227-b83d-54dc13a838d3.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 76 of 79 · 1,561 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Rugby Regular Strength Acetaminophen	ACETAMINOPHEN	A-S Medication Solutions	400d4a29-9e39-4e74-8272-37be5d789924	2023-11-22	Warnings	Exact identifier application number: M013
RIGHT REMEDIES Pain Relief Extra Strength Caplet	ACETAMINOPHEN	Strive Pharmaceuticals Inc.	dcce28d9-8528-489e-b995-1d98e9d0e6ad	2023-11-21	Warnings	Exact identifier application number: M013
Sanatos Multi Symptom Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCI	Pharmadel LLC	0ab11691-5b29-55fc-e063-6394a90aa328	2023-11-17	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	A-S Medication Solutions	1e223faa-f6d0-4235-bc4c-6cfca84a5b0a	2023-11-17	Warnings	Exact identifier application number: M013
SanaTos X	ACETAMINOPHEN, DEXTROMETHORPHAN HBR,GUAIFENESIN, PHENYLEPHRINE HCI	Pharmadel LLC	85b8ef3d-7318-7f3b-e053-2991aa0a0777	2023-11-14	Warnings	Exact identifier application number: M013
RIGHT REMEDIES EXTRA STRENGTH PM Pain Relief	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Strive Pharmaceuticals Inc.	8badbaad-eb35-4251-a779-00474819360d	2023-11-13	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Trifecta Pharmaceuticals USA LLC	09935a74-34b0-0e7c-e063-6294a90a7c83	2023-11-07	Warnings	Exact identifier application number: M013
Pain Relief PM	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	AMERIFOODS TRADING COMPANY	f6dd6396-93e9-1096-e053-6394a90af06d	2023-11-02	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	RETAIL BUSINESS SERVICES , LLC.	eb644e9e-36dc-5f84-e053-2a95a90affa5	2023-11-02	Warnings	Exact identifier application number: M013
Good Sense Childrens Pain and Fever	ACETAMINOPHEN	Proficient Rx LP	46527b1f-7515-44ce-b5cb-9d24223b9af1	2023-11-01	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	A-S Medication Solutions	12feb32b-4b8c-4b17-9e86-cb286457b088	2023-11-01	Warnings	Exact identifier application number: M013
Acetaminophen, Aspirin, Caffeine	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Proficient Rx LP	af8b30a0-7a56-4557-8404-cc8059fcd6bc	2023-11-01	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	AMERIFOODS TRADING COMPANY	f6dd387d-c768-9443-e053-6394a90aca14	2023-10-31	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	AMERIFOODS TRADING COMPANY	f6cec280-17a5-5c5d-e053-6394a90a81aa	2023-10-31	Warnings	Exact identifier application number: M013
Regular Strength Aspirin	ASPIRIN	CARDINAL HEALTH, INC.	8aaa82c6-b46b-25c5-e053-2a95a90a3793	2023-10-30	Warnings	Exact identifier application number: M013
SafeTynadol	ACETAMINOPHEN	Sinew Pharma Inc.	b956d527-7ea7-e084-e053-2a95a90a866d	2023-10-28	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Magno-Humphries, Inc.	9d2275c8-0c3d-d2b3-e053-2995a90a368e	2023-10-27	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	Magno-Humphries, Inc.	9d22bedb-9fb3-8421-e053-2a95a90acf4a	2023-10-27	Warnings	Exact identifier application number: M013
Acetaminophen Regular Strength	ACETAMINOPHEN	Magno-Humphries, Inc.	9d22d642-8aaf-d17e-e053-2995a90ae182	2023-10-27	Warnings	Exact identifier application number: M013
ENTERIC COATED ASPIRIN	ASPIRIN	Magno-Humphries, Inc.	a7c02378-4213-4e57-aca2-2437ad02f786	2023-10-27	Warnings	Exact identifier application number: M013

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
308416	aspirin 81 MG Delayed Release Oral Tablet	PSN	b4064039-2345-4227-b83d-54dc13a838d3	24
308416	aspirin 81 MG Delayed Release Oral Tablet	SCD	b4064039-2345-4227-b83d-54dc13a838d3	24
308416	ASA 81 MG Delayed Release Oral Tablet	SY	b4064039-2345-4227-b83d-54dc13a838d3	24
308416	aspirin 81 MG Enteric Coated Oral Tablet	SY	b4064039-2345-4227-b83d-54dc13a838d3	24

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55910-600-32	55910060032	1 BOTTLE, PLASTIC in 1 CARTON (55910-600-32) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC		2011-05-01	0000-00-00	No	No	Current
55910-600-69	55910060069	1 BOTTLE in 1 CARTON (55910-600-69) > 144 TABLET, COATED in 1 BOTTLE	1 bottle	2011-05-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Dollar General 44-600A	DOLGENCORP, LLC \| LNK International, Inc.	2026-08-07	HUMAN OTC DRUG LABEL	25