CorePharma, LLC OTC
FDA Approved Drugs

CorePharma, LLC OTC

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

OTC
  • Total Records 1
  • Latest Approval Date Aug 22, 2019
  • Data Source FDA
  • First Approval Date Aug 22, 2019
All
73
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Unclassified
6
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Discontinued
10
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OTC
1
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RX
56
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Company Overview

Company

CorePharma, LLC OTC

Country

U.S.A

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Company Snapshot

CorePharma, LLC OTC

215 Wood Avenue, Middlesex, NJ 08846

U.S.A

www.corepharma.com/ customer.service@corepharma.com View on Map
FDA Approved Drug Records ( 1 record )
2019
22 Aug
OTC Application: 211830

Drug Name

NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG;220MG

Approval Date

2019-08-22

211830 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

Application Number

211830

Product Number

1

Dosage Form

-

Strength

25MG;220MG

Approval Date

2019-08-22

Regulatory Status

OTC

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Drug Status Breakdown
1 total
  • OTC
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

211830

Product Number

1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

Dosage Form

-

Strength

25MG;220MG

FDA Approved Drug Data

Approved drug product information

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