ASPIRIN

Product NDC: 59779-945
11-digit product format: 597790945
Labeler code: 59779
Product ID: 59779-945_306e0e90-2dfe-4b85-8ddf-c3b2ae09035b
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: CVS Pharmacy
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-07-25
Marketing end: 2027-05-31
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
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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	59779-945	59779-945-07	D	Discontinued by firm	2026-10-15
excluded package	package	59779-945	59779-945-17	D	Discontinued by firm	2026-10-15
excluded package	package	59779-945	59779-945-32	D	Discontinued by firm	2026-10-15

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 · 25 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	59779-945-17	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	59779-945-07	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	59779-945-32	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	59779-945-17	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	59779-945-07	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	59779-945-07	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	59779-945-17	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	59779-945-07	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	59779-945-17	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	59779-945-07	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	59779-945-17	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	59779-945-07	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	59779-945-17	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	59779-945-07	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	59779-945-17	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	59779-945-07	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	59779-945-17	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	59779-945-07	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	59779-945-17	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	59779-945-07	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	59779-945-17	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	59779-945-07	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	59779-945-17	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	59779-945-07	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	59779-945-17	`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
Brand name suffix: Low Strength

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
6e1c1129-562b-4a8a-ac37-db3cb2a82735	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
59779-945-07	ASPIRINLow Strength	36 in 1 BOTTLE	TABLET, DELAYED RELEASE	36	18
59779-945-07	ASPIRINLow Strength	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	18
59779-945-17	ASPIRINLow Strength	300 in 1 BOTTLE	TABLET, DELAYED RELEASE	300	18
59779-945-17	ASPIRINLow Strength	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	18
59779-945-32	ASPIRINLow Strength	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	18
59779-945-32	ASPIRINLow Strength	120 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	120	18
59779-945-51	ASPIRINLow Strength	365 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	365	18

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59779-945-32	EA - Each	59779-945	532de589-1fb1-400a-bbf1-6a30ae69cae9	1	2017-09-11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
METHACRYLIC ACID	INACTIVE INGREDIENT	1CS02G8656	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
SHELLAC	INACTIVE INGREDIENT	46N107B71O	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-945	ASPIRIN LOW STRENGTH (ASPIRIN) TABLET, DELAYED RELEASE [CVS PHARMACY]	16	Current NDC, Legacy NDC, 7 package rows	20240718_6e1c1129-562b-4a8a-ac37-db3cb2a82735.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 34 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Walmart Inc.	1557bd9b-3e7c-4769-e063-6394a90a9d91	2025-11-04	Warnings	Exact identifier application number: M013
Adult Low Dose Aspirin	ASPIRIN	Rising Pharma Holdings, Inc.	c3c4854e-726e-4926-b044-a5094943c306	2025-11-04	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	HYVEE INC	3e50b3f6-1e1a-41b9-e063-6394a90abe36	2025-11-03	Warnings	Exact identifier application number: M013
Good Sense Pain Relief	ACETAMINOPHEN	L. Perrigo Company	447de441-7d28-4415-81c5-4fc05622dd05	2025-11-03	Warnings	Exact identifier application number: M013
Children Acetaminophen Oral Solution	ACETAMINOPHEN	VERITYRX. LLC	42a17f54-7851-84fb-e063-6394a90a9ec1	2025-11-02	Warnings	Exact identifier application number: M013
M-PAP	ACETAMINOPHEN	VERITYRX, LLC	42a1a128-a2dd-bbc9-e063-6294a90a4fe1	2025-11-02	Warnings	Exact identifier application number: M013
Physicians Care Aspirin	ASPIRIN	Acme United Corporation	aa67ea3a-2741-7ee0-e053-2a95a90a6485	2025-10-31	Warnings	Exact identifier application number: M013
PhysiciansCare Non Aspirin Extra Strength	ACETAMINOPHEN	Acme United Corporation	c7006775-bd5b-412f-963d-ce5a158216c5	2025-10-31	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	Walgreens	f7aa624b-b00c-4fd3-9965-8e4d2b3eb4ba	2025-10-31	Warnings	Exact identifier application number: M013
Extra Strength Acetaminophen	ACETAMINOPHEN	NuCare Pharmaceuticals, Inc.	41affa1a-5aac-7fc0-e063-6394a90a5557	2025-10-30	Warnings	Exact identifier application number: M013
MAPAP Extra Strength	ACETAMINOPHEN	Major Pharmaceuticals	34a95450-3f04-4de4-9113-73e7bd5724a0	2025-10-29	Warnings	Exact identifier application number: M013
GOODNOW PAIN RELIEF	ACETAMINOPHEN	Gobrands, Inc	4d4a78a5-5a88-4f24-b685-c7c6bb5e989e	2025-10-29	Warnings	Exact identifier application number: M013
Sanaflu Xtra	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	GRANDALL DISTRIBUTING, LLC	4af8a566-5251-4d46-8692-87a3a0748334	2025-10-28	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Rising Pharma Holdings, Inc.	f8237772-7656-49fb-b1de-f8fcb5fa55ee	2025-10-28	Warnings	Exact identifier application number: M013
DG Health Pain Relief	ACETAMINOPHEN	Dolgencorp Inc	42f0c87c-7020-4af7-9f6b-3a774137e564	2025-10-24	Warnings	Exact identifier application number: M013
GOODYS Hangover	ASPIRIN AND CAFFEINE	Medtech Products Inc.	0b0067e0-58b0-4581-aa4b-e398c32c559a	2025-10-23	Warnings	Exact identifier application number: M013
GOODYS Extra Strength Headache Mixed Fruit Blast	ACETAMINOPHEN, ASPIRIN, AND CAFFEINE	Medtech Products Inc.	6cb758bf-5a50-46bb-96e7-65b810b12de0	2025-10-23	Warnings	Exact identifier application number: M013
Nyt Time Sleep Caps	DIPHENHYDRAMINE HYDROCHLORIDE	DISCOUNT DRUG MART	e3f4d063-921d-4503-89a6-26cc9c46b4c9	2025-10-23	Warnings	Exact identifier application number: M013
Anacin	ASPRIN AND CAFFEINE	Insight Pharmaceuticals LLC	51ab0ee3-3c94-424d-a30a-2d6c14e3d8ff	2025-10-23	Warnings	Exact identifier application number: M013
Goodys Back and Body Pain	ACETAMINOPHEN AND ASPRIN	Medtech Products Inc.	055d0288-61d4-48bc-b91f-6ecc1969beb8	2025-10-23	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	6e1c1129-562b-4a8a-ac37-db3cb2a82735	18
308416	aspirin 81 MG Delayed Release Oral Tablet	SCD	6e1c1129-562b-4a8a-ac37-db3cb2a82735	18
308416	ASA 81 MG Delayed Release Oral Tablet	SY	6e1c1129-562b-4a8a-ac37-db3cb2a82735	18
308416	aspirin 81 MG Enteric Coated Oral Tablet	SY	6e1c1129-562b-4a8a-ac37-db3cb2a82735	18

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
59779-945-07	59779094507	36 in 1 BOTTLE					Historical
59779-945-17	59779094517	300 in 1 BOTTLE					Historical
59779-945-32	59779094532	1 BOTTLE, PLASTIC in 1 CARTON (59779-945-32) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC	2014-07-25	0000-00-00	No	No	Current
59779-945-51	59779094551	365 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (59779-945-51)	2014-07-25	2027-05-31	No	No	Current