Extra Strength Acetaminophen

Product NDC: 57896-204
11-digit product format: 578960204
Labeler code: 57896
Product ID: 57896-204_45257b9e-6003-5356-e063-6294a90a1af0
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET
Route: ORAL
Labeler: Geri-Care Pharmaceutical Corp
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-07-01
Marketing end: 2027-02-28
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	57896-204	57896-204-10	D	Discontinued by firm		2026-10-21

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 · 1 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	57896-204	57896-204-10	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

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: Extra Strength Acetaminophen

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
362O9ITL9D	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198440	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
7a29dde6-a177-6206-e053-2991aa0a01f2	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
57896-204-01	Extra Strength Acetaminophen	100 in 1 BOTTLE	TABLET	100	7
57896-204-05	Extra Strength Acetaminophen	50 in 1 BOTTLE	TABLET	50	7
57896-204-10	Extra Strength Acetaminophen	1000 in 1 BOTTLE	TABLET	1000	7
57896-204-20	Extra Strength Acetaminophen	200 in 1 BOTTLE	TABLET	200	7

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
57896-204-01	EA - Each	57896-204	5b5981d9-4c39-4d62-9bb3-1944ee83a128	1	2018-12-13
57896-204-05	EA - Each	57896-204	0ef19d63-6981-46b8-a80e-e204eb7dc370	1	2021-06-02
57896-204-20	EA - Each	57896-204	a4fc79ba-8933-4ac1-9056-046d8a6d1c3b	1	2022-03-09

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57896-204	EXTRA STRENGTH ACETAMINOPHEN (ACETAMINOPHEN) TABLET [GERI-CARE PHARMACEUTICAL CORP]	6	Current NDC, Legacy NDC, 4 package rows	20241129_7a29dde6-a177-6206-e053-2991aa0a01f2.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 78 of 79 · 1,576 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Regular Strength Pain Reliever	ACETAMINOPHEN	INGLES MARKETS, INC.	f06fe167-8a16-14d9-e053-2a95a90a1a0f	2023-10-17	Warnings	Exact identifier application number: M013
Childrens Chewable Acetaminophen	ACETAMINOPHEN	BLESSINGS INTERNATIONAL	ee8ba190-2c42-7ca2-e053-2a95a90a01a0	2023-10-17	Warnings	Exact identifier application number: M013
Aphen	ACETAMINOPHEN	Asclemed USA, Inc.	fe3c0a2b-316b-4620-b6bc-378dbaf7ed57	2023-10-16	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN	Walgreens	b4b06d32-6a09-4c43-980b-377b617ba739	2023-10-09	Warnings	Exact identifier application number: M013
FLO PMS Complete	ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE	O Positiv, Inc.	cce62d9f-adb1-4473-8258-910dff6b1378	2023-10-09	Warnings	Exact identifier application number: M013
childrens mapap	ACETAMINOPHEN	Proficient Rx LP	88c4183a-3032-46de-bf18-f700055f617b	2023-10-01	Warnings	Exact identifier application number: M013
Tri-Buffered Aspirin	ASPIRIN	Proficient Rx LP	640c3311-2abf-40b2-82b9-9fe4d8c1cf1d	2023-10-01	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	CVS PHARMACY, INC	852e70e2-7279-6f33-e053-2991aa0a8676	2023-08-28	Warnings	Exact identifier application number: M013
Children Pain Relief	CHILDREN PAIN RELIEF	Allegiant Health	44c90cbe-8ece-4dd8-9ea5-7f8d6f4c0096	2023-07-17	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	Better Living Brands LLC	4a76e898-3204-4f77-bc67-c19f5fe829f3	2023-07-05	Warnings	Exact identifier application number: M013
Aspirin Enteric Coated	ASPIRIN 81 MG	Lodaat LLC	04017bc9-602a-4204-96a9-b7f9713155f6	2023-01-31	Warnings	Exact identifier application number: M013
Aspirin 325 mg	ASPIRIN	WALGREENS	d71a22e8-9e39-a672-e053-2a95a90a1403	2022-07-08	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	PAIN RELIEF	Allegiant Health	d41d2319-8eed-4df9-813c-313497ceb8b4	2021-11-23	Warnings	Exact identifier application number: M013
Pain Relief PM Extra Strength	PAIN RELIEF PM	Allegiant Health	4c9969be-a01f-4ca4-800a-e404229ce28b	2021-11-23	Warnings	Exact identifier application number: M013
Tension Headache Relief	TENSION HEADACHE RELIEF	Allegiant Health	9d348550-060b-410f-8c1e-8f43d00b860e	2021-11-22	Warnings	Exact identifier application number: M013
Aspirin 81mg Enteric coated Low Strength Aspirin Regimen	ASPIRIN	Allegiant Health	847fd2f8-2e32-4ef2-a793-b902045110f1	2021-11-19	Warnings	Exact identifier application number: M013
Aspirin 81mg Enteric coated Delayed Release	ASPIRIN	Allegiant Health	d6c7c8c9-b997-4acc-a066-133bfb1239cb	2021-11-02	Warnings	Exact identifier application number: M013
Aspirin 81mg Enteric coated Delayed Release	ASPIRIN	Dr. Wayne's	eacbdf9e-5642-4986-a03c-b0812d28265d	2021-11-02	Warnings	Exact identifier application number: M013
Aspirin 81mg Enteric coated Low Strength Aspirin Regimen	ASPIRIN	Allegiant Health	d9abe780-7e58-43d8-848f-c6c8893aea2e	2021-10-14	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN 500MG	Allegiant Health	0f72be92-fac0-4be4-87a3-3f20f0f01db5	2021-05-17	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198440	acetaminophen 500 MG Oral Tablet	PSN	ea417ddb-54b3-49e2-bec1-8fe450d9990c	101
198440	acetaminophen 500 MG Oral Tablet	SCD	ea417ddb-54b3-49e2-bec1-8fe450d9990c	101
198440	APAP 500 MG Oral Tablet	SY	ea417ddb-54b3-49e2-bec1-8fe450d9990c	101
198440	acetaminophen 500 MG Oral Tablet	PSN	7a29dde6-a177-6206-e053-2991aa0a01f2	7
198440	acetaminophen 500 MG Oral Tablet	SCD	7a29dde6-a177-6206-e053-2991aa0a01f2	7
198440	APAP 500 MG Oral Tablet	SY	7a29dde6-a177-6206-e053-2991aa0a01f2	7
198440	acetaminophen 500 MG Oral Tablet	PSN	e72bf35b-acc9-3562-e053-2995a90aeff3	1
198440	acetaminophen 500 MG Oral Tablet	SCD	e72bf35b-acc9-3562-e053-2995a90aeff3	1
198440	APAP 500 MG Oral Tablet	SY	e72bf35b-acc9-3562-e053-2995a90aeff3	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
57896-204-01	57896020401	100 TABLET in 1 BOTTLE (57896-204-01)	100 tablet	2018-07-01	2027-02-28	No	No	Current
57896-204-05	57896020405	50 TABLET in 1 BOTTLE (57896-204-05)	50 tablet	2018-07-01	2027-02-28	No	No	Current
57896-204-10	57896020410	1000 TABLET in 1 BOTTLE (57896-204-10)	1000 tablet	2018-07-01	0000-00-00	No	No	Current
57896-204-20	57896020420	200 TABLET in 1 BOTTLE (57896-204-20)	200 tablet	2018-07-01	2026-10-31	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
gc204	Bryant Ranch Prepack	2026-03-19	HUMAN OTC DRUG LABEL	101
gc204	Geri-Care Pharmaceutical Corp	2025-12-04	HUMAN OTC DRUG LABEL	7
ACETAMINOPHEN	Direct_Rx	2023-07-20	HUMAN OTC DRUG LABEL	3
gc204	NuCare Pharmaceuticals,Inc.	2022-08-26	HUMAN OTC DRUG LABEL	1
gc204	Bryant Ranch Prepack	2022-02-14	HUMAN OTC DRUG LABEL	3
gc204	Preferred Pharmaceuticals, Inc.	2021-05-04	HUMAN OTC DRUG LABEL	2
Acetaminophen - NuCare Pharmaceuticals,Inc.	NuCare Pharmaceuticals,Inc.	2021-04-15	HUMAN OTC DRUG LABEL	1