Low Dose Aspirin

Product NDC: 49035-563
11-digit product format: 490350563
Labeler code: 49035
Product ID: 49035-563_ea158083-c7a0-4b01-aa1d-d0e41bdc5e70
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: Wal-Mart Stores Inc
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	49035-563	49035-563-27	D	Discontinued by firm		2026-10-05
excluded package	package	49035-563	49035-563-96	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 · 21 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	49035-563-96	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	49035-563-27	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	49035-563-96	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	49035-563-27	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	49035-563-27	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	49035-563-96	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	49035-563-27	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	49035-563-96	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	49035-563-27	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	49035-563-96	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	49035-563-27	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	49035-563-96	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	49035-563-27	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	49035-563-96	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	49035-563-27	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	49035-563-96	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	49035-563-27	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	49035-563-96	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	49035-563-27	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	49035-563-27	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	49035-563-27	`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: Low Dose Aspirin
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
093e0458-9975-456f-8950-8273c8890b3c	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
594e2c86-3079-4e6e-96c9-48f7a8afc78d	Product name	1	20230718
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
49035-563-11	Low Dose Aspirin	60 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	60	20
49035-563-11	Low Dose Aspirin	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	20
49035-563-13	Low Dose Aspirin	250 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	250	20
49035-563-13	Low Dose Aspirin	2 in 1 CARTON	TABLET, DELAYED RELEASE	2	20
49035-563-14	Low Dose Aspirin	500 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	500	20
49035-563-17	Low Dose Aspirin	300 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	300	20
49035-563-27	Low Dose Aspirin	32 in 1 BOTTLE	TABLET, DELAYED RELEASE	32	20
49035-563-27	Low Dose Aspirin	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	20
49035-563-32	Low Dose Aspirin	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	20
49035-563-32	Low Dose Aspirin	120 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	120	20
49035-563-96	Low Dose Aspirin	250 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	250	20
49035-563-96	Low Dose Aspirin	2 in 1 CARTON	TABLET, DELAYED RELEASE	2	20

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49035-563-11	EA - Each	49035-563	ebec318f-1f12-41f5-a80f-930e60b07c71	1	2023-04-07
49035-563-14	EA - Each	49035-563	cd68088e-ceaf-4855-b61c-e46423863505	1	2016-03-04
49035-563-17	EA - Each	49035-563	f22db8dc-c419-4a04-98ef-288aa123113b	1	2013-02-13
49035-563-32	EA - Each	49035-563	245bd25d-686d-4f7d-80b2-d950025d4813	1	2013-10-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
METHACRYLIC ACID	INACTIVE INGREDIENT	1CS02G8656	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
SHELLAC	INACTIVE INGREDIENT	46N107B71O	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-563	LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [WAL-MART STORES INC]	19	Current NDC, Legacy NDC, 12 package rows	20250519_093e0458-9975-456f-8950-8273c8890b3c.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 8 of 83 · 1,657 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Extra Strength Acetaminophen	ACETAMINOPHEN	Hi-Tech Nutraceuticals, LLC	a36be487-7a36-550f-e053-2a95a90a95c1	2026-07-06	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Hi-Tech Nutraceuticals, LLC	a39c524e-c131-d7fb-e053-2995a90a785b	2026-07-06	Warnings	Exact identifier application number: M013
PAIN RELIEVER	ASPIRIN 81 MG	Health Pharma USA, LLC	d60aed37-3a9e-46d1-e053-2995a90a1d1f	2026-07-06	Warnings	Exact identifier application number: M013
Tylenol PM Extra Strength	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	Select Consumer Group	55d0dceb-c9a9-778e-e063-6294a90a2ad7	2026-07-04	Warnings	Exact identifier application number: M013
Bayer Genuine Aspirin	ASPIRIN	Select Consumer Group	3ca776c2-47ed-5107-e063-6394a90ac5df	2026-07-03	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Rugby Laboratories	f7ca9f4a-f8ef-46d2-9536-b69541e6653d	2026-07-02	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	United Natural Foods, Inc. dba UNFI	19c7f832-d7ec-4dcc-8aa4-f4cbf64c9ff6	2026-07-02	Warnings	Exact identifier application number: M013
Regular Strength Enteric coated aspirin	ASPIRIN	St. Mary's Medical Park Pharmacy	33733144-b26a-b4a3-e063-6294a90ae049	2026-07-01	Warnings	Exact identifier application number: M013
pain relief EXTRA STRENGTH	ACETAMINOPHEN	Meijer Distribution, Inc.	ae84eb7e-a70b-4311-b2dc-ad153047a516	2026-07-01	Warnings	Exact identifier application number: M013
Aspirin 325 mg	ASPIRIN	Hi-Tech Nutraceuticals, LLC	b3426a9a-ea99-da30-e053-2995a90a1e4b	2026-07-01	Warnings	Exact identifier application number: M013
Headache Relief Extra Strength	ACETAMINOPHEN, ASPIRIN AND CAFFEINE	Salado Sales, Inc.	ca21d576-be3c-495d-9dbd-ed514bf65da7	2026-07-01	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Meijer Distribution Inc	4e08a7cb-3894-84c3-e063-6394a90a0b42	2026-06-30	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	St. Mary's Medical Park Pharmacy	0cca91cb-f05b-3cf8-e063-6394a90a9f79	2026-06-30	Warnings	Exact identifier application number: M013
Headache Relief Extra Strength	ACETAMINOPHEN, ASPIRIN AND CAFFEINE	Wal-Mart Stores Inc	9b1201af-c802-4e19-b192-bbbf34367db4	2026-06-30	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	P & L Development, LLC	fc841cba-8f4f-407b-97de-0422977515bd	2026-06-30	Warnings	Exact identifier application number: M013
Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	United Natural Foods, Inc. dba UNFI	b6ff2b34-51ee-41bc-8b7d-7520ade0bf36	2026-06-30	Warnings	Exact identifier application number: M013
Medline	ASPIRIN	Medline Industries, LP	4b0c569a-ed7a-e104-e063-6394a90a6d54	2026-06-29	Warnings	Exact identifier application number: M013
Extra Strength Pain Relief	ACETAMINOPHEN	St. Mary's Medical Park Pharmacy	31ce5c80-152f-12a1-e063-6394a90ab119	2026-06-29	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	WALMART INC.	e50b3f60-b827-426c-8e78-8447c89130fe	2026-06-29	Warnings	Exact identifier application number: M013
Acetaminophen PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Chain Drug Marketing Association, Inc.	e58417f4-3575-4433-ac2e-b7bf9fe8ba10	2026-06-29	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	093e0458-9975-456f-8950-8273c8890b3c	20
308416	aspirin 81 MG Delayed Release Oral Tablet	SCD	093e0458-9975-456f-8950-8273c8890b3c	20
308416	ASA 81 MG Delayed Release Oral Tablet	SY	093e0458-9975-456f-8950-8273c8890b3c	20
308416	aspirin 81 MG Enteric Coated Oral Tablet	SY	093e0458-9975-456f-8950-8273c8890b3c	20

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49035-563-11	49035056311	1 BOTTLE, PLASTIC in 1 CARTON (49035-563-11) / 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC		2011-05-01	0000-00-00	No	No	Current
49035-563-13	49035056313	2 BOTTLE, PLASTIC in 1 CARTON (49035-563-13) / 250 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC		2011-05-01	2027-04-30	No	No	Current
49035-563-14	49035056314	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49035-563-14)		2011-05-01	0000-00-00	No	No	Current
49035-563-17	49035056317	300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49035-563-17)		2011-05-01	0000-00-00	No	No	Current
49035-563-27	49035056327	1 BOTTLE in 1 CARTON (49035-563-27) > 32 TABLET in 1 BOTTLE	1 bottle	2011-05-01	0000-00-00	No	No	Current
49035-563-32	49035056332	1 BOTTLE, PLASTIC in 1 CARTON (49035-563-32) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC		2011-05-01	0000-00-00	No	No	Current
49035-563-96	49035056396	2 BOTTLE in 1 CARTON (49035-563-96) > 250 TABLET in 1 BOTTLE	2 bottle	2011-05-01	0000-00-00	No	No	Current