Acetaminophen

Product NDC: 76168-120
11-digit product format: 761680120
Labeler code: 76168
Product ID: 76168-120_6c311047-4be7-44ad-e053-2a91aa0ad047
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET
Route: ORAL
Labeler: Velocity Pharma LLC
Application: part343
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2018-05-14
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Acetaminophen
Listing expiration: 2026-12-31

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
bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76168-120-10	Acetaminophen	60 in 1 BOTTLE	TABLET	60		2
76168-120-10	Acetaminophen	1 in 1 CARTON	TABLET	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76168-120	ACETAMINOPHEN TABLET [VELOCITY PHARMA LLC]	2	Current NDC, Legacy NDC, 2 package rows	20180515_bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acetaminophen	ACETAMINOPHEN	Velocity Pharma LLC	bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50	2018-05-14	Warnings	Exact identifier ndc (product): 76168-120

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	bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50	2
198440	acetaminophen 500 MG Oral Tablet	SCD	bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50	2
198440	APAP 500 MG Oral Tablet	SY	bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76168-120-10	76168012010	60 CARTON in 1 BOTTLE (76168-120-10) / 1 TABLET in 1 CARTON	60 carton	2018-05-14	0000-00-00	No	No	Current