Aspirin

Product NDC: 57344-080
11-digit product format: 573440080
Labeler code: 57344
Product ID: 57344-080_1ac8cf0e-4f03-ff3f-e063-6394a90a5c61
Type: HUMAN OTC DRUG
Nonproprietary name: ASPIRIN
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: AAA Pharmaceutical, Inc.
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-07-01
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: 2026-12-31
Current FDA listing: Yes

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
Listing expiration: 2026-12-31

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
609948d6-0f20-4d0c-adc0-6ae72a4f2b7a	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d7724692-1155-4cc8-a415-22f5fc4aec35	Product name	6	20220216
bde672ba-4805-28d0-1986-73543d41b412	Product name	2	20210201
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
ade821ba-260a-47e2-bd89-743e27ac9906	Product name	1	20161121
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657	Product name	1	20150929
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
57344-080-01	Aspirin	120 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	120	4
57344-080-01	Aspirin	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	4
57344-080-20	Aspirin	300 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	300	4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
ANHYDROUS LACTOSE	INACTIVE INGREDIENT	3SY5LH9PMK	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
BROWN IRON OXIDE	INACTIVE INGREDIENT	1N032N7MFO	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
CARNAUBA WAX	INACTIVE INGREDIENT	R12CBM0EIZ	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
DIACETYLATED MONOGLYCERIDES	INACTIVE INGREDIENT	5Z17386USF	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
DIMETHICONE	INACTIVE INGREDIENT	92RU3N3Y1O	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST)	INACTIVE INGREDIENT	87Y6436BKR	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)	INACTIVE INGREDIENT	74G4R6TH13	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
MINERAL OIL	INACTIVE INGREDIENT	T5L8T28FGP	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57344-080	ASPIRIN TABLET, DELAYED RELEASE [AAA PHARMACEUTICAL, INC.]	4	Current NDC, Legacy NDC, 3 package rows	20240615_609948d6-0f20-4d0c-adc0-6ae72a4f2b7a.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 33 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
EXTRA STRENGTH PAIN RELIEVER	ACETAMINOPHEN, ASPIRIN AND CAFFEINE	Geri-Care Pharmaceutical Corp	b670a898-2360-76e2-e053-2a95a90a3380	2025-11-17	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	L.N.K. International, Inc.	ec902e52-0f48-4a61-b67d-17e1c1461619	2025-11-15	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN	L.N.K. International, Inc.	72babe91-2586-4f05-ae90-6debfd23aa5d	2025-11-15	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	Strategic Sourcing Services LLC	3c7883da-6f51-4716-b012-0e33d239a60e	2025-11-15	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	Sam's West Inc	3b84746f-05ab-4f88-b9ae-efb8c5dfc233	2025-11-15	Warnings	Exact identifier application number: M013
Childrens Pain and Fever	ACETAMINOPHEN	Walgreen Company	a482e715-bec0-44a4-bb0e-ea5f5fda558e	2025-11-15	Warnings	Exact identifier application number: M013
Acetaminophen PM Extra Strength	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	ARMY AND AIR FORCE EXCHANGE SERVICE	f1157dbc-d86c-4554-954c-60a74674ff6b	2025-11-15	Warnings	Exact identifier application number: M013
Acetaminophen, Aspirin, Caffeine	ACETAMINOPHEN, ASPIRIN, CAFFEINE	NuCare Pharmaceuticals,Inc.	437e4fd9-c7d9-77d6-e063-6294a90a22b7	2025-11-13	Warnings	Exact identifier application number: M013
Good Sense Pain Relief	ACETAMINOPHEN	L. Perrigo Company	7f78028a-484b-48b3-a37a-1e0b055bbefc	2025-11-13	Warnings	Exact identifier application number: M013
OneSsip Acetaminophen	ACETAMINOPHEN	MEDWISE LIFESCIENCES INC.	3f88de0f-6cf6-3580-e063-6294a90abcb4	2025-11-12	Warnings	Exact identifier application number: M013
Tylenol PM Extra Strength	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	Navajo Manufacturing Company Inc.	435b1a31-353d-af20-e063-6294a90aa907	2025-11-11	Warnings	Exact identifier application number: M013
Good Neighbor Pharmacy Pain Relief	ACETAMINOPHEN	Amerisource Bergen	4b829607-f5fb-427f-83b5-5b6b9c44ebeb	2025-11-11	Warnings	Exact identifier application number: M013
Pamprin Max Menstrual Pain Relief	ACETAMINOPHEN AND ASPIRIN AND CAFFEINE	Focus Consumer Healthcare, LLC	5bd4b935-f003-7df8-e053-2a91aa0a5d79	2025-11-10	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	Shield Pharmaceuticals Corp	61e50135-a7c2-4a86-8a1a-d47b41d3f9d1	2025-11-07	Warnings	Exact identifier application number: M013
Childrens Chewables	ACETAMINOPHEN	Strategic Sourcing Services LLC	af2cbbaf-9b73-440a-bc88-a790cafccc6b	2025-11-07	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	L.N.K. International, Inc.	39e142a7-8590-4e1e-8319-6904fb57cc8a	2025-11-06	Warnings	Exact identifier application number: M013
TYLENOL Extra Strength	ACETAMINOPHEN	Kenvue Brands LLC	42321456-d7dd-3b51-e063-6394a90ac292	2025-11-05	Warnings	Exact identifier application number: M013
Childrens Pain Relief	ACETAMINOPHEN	Family Dollar Services Inc	76058eb3-2d3f-4414-87df-7167cd27d26b	2025-11-05	Warnings	Exact identifier application number: M013
Children Pain and Fever Reliver	ACETAMINOPHEN	Target Corporation	1116f808-f61e-47ec-b0d0-d4be5aa905be	2025-11-04	Warnings	Exact identifier application number: M013
Pain Reliever Dye Free	ACETAMINOPHEN	TIME CAP LABORATORIES, INC.	42c4f0b2-6483-0f3c-e063-6294a90a140f	2025-11-04	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	609948d6-0f20-4d0c-adc0-6ae72a4f2b7a	4
308416	aspirin 81 MG Delayed Release Oral Tablet	SCD	609948d6-0f20-4d0c-adc0-6ae72a4f2b7a	4
308416	ASA 81 MG Delayed Release Oral Tablet	SY	609948d6-0f20-4d0c-adc0-6ae72a4f2b7a	4
308416	aspirin 81 MG Enteric Coated Oral Tablet	SY	609948d6-0f20-4d0c-adc0-6ae72a4f2b7a	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
57344-080-01	57344008001	1 BOTTLE, PLASTIC in 1 CARTON (57344-080-01) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC	2017-07-01	0000-00-00	No	No	Current
57344-080-20	57344008020	300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (57344-080-20)	2024-03-15		No	No	Current