Paracetamol Human Otc Drug - NDC Database

NDC Database
Elysium Pharmaceuticals Ltd.
Paracetamol Human Otc Drug

Paracetamol Human Otc Drug

National Drug Code (NDC) records including drug products, labelers, dosage forms, strengths, substances and marketing information.

HUMAN OTC DRUG
Last Marketing Date
2024-03-07
Data Source
FDA
First Marketing Date
2024-01-30
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NDC Records Timeline (4 records)
Clear
2024
07 Mar
Elysium Pharmaceuticals Ltd.
HUMAN OTC DRUG

NDC

14803-013

Labeler

Elysium Pharmaceuticals Ltd.

Nonproprietary Name

Acetaminophen

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET

Strength

325 mg/1

Start Marketing: 2024-03-07

Substance

ACETAMINOPHEN

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-03-07

End Marketing Date

-

Listing / Certification

2027-12-31

2024
07 Mar
Elysium Pharmaceuticals Ltd.
HUMAN OTC DRUG

NDC

14803-281

Labeler

Elysium Pharmaceuticals Ltd.

Nonproprietary Name

Acetaminophen

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET

Strength

500 mg/1

Start Marketing: 2024-03-07

Substance

ACETAMINOPHEN

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-03-07

End Marketing Date

-

Listing / Certification

2026-12-31

2024
07 Mar
Elysium Pharmaceuticals Ltd.
HUMAN OTC DRUG

NDC

14803-281

Labeler

Elysium Pharmaceuticals Ltd.

Nonproprietary Name

Acetaminophen

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET

Strength

500 mg/1

Start Marketing: 2024-03-07

Substance

ACETAMINOPHEN

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-03-07

End Marketing Date

-

Listing / Certification

2027-12-31

2024
30 Jan
Elysium Pharmaceuticals Ltd.
HUMAN OTC DRUG

NDC

14803-282

Labeler

Elysium Pharmaceuticals Ltd.

Nonproprietary Name

Acetaminophen and Diphenhydramine Hydrochloride

Marketing Category

DRUG FOR FURTHER PROCESSING

Dosage Form

TABLET

Strength

500; 25 mg/1; mg/1

Start Marketing: 2024-01-30

Substance

ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-01-30

End Marketing Date

-

Listing / Certification

2027-12-31

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Related Databases
5 of 6 have records
Product Type Breakdown
4 total
  • HUMAN OTC DRUG
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

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Record Details Preview

Click "View Details" on any record above to expand full details inline.

Substance

ACETAMINOPHEN

Identifiers

NDC: 14803-013
DEA Schedule:

Official FDA Data

Based on publicly available FDA NDC information

National Drug Code

Structured NDC product information

Product Information

Drug, labeler and marketing data

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NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.
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