Norwich Pharmaceuticals Inc. Discontinued
FDA Approved Drugs

Norwich Pharmaceuticals Inc. Discontinued

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.

Discontinued
  • Total Records 3
  • Latest Approval Date Apr 21, 1993
  • Data Source FDA
  • First Approval Date Apr 21, 1993
All
13
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Unclassified
1
View
Discontinued
3
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RX
9
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Company Overview

Company

Norwich Pharmaceuticals Inc. Discontinued

Country

U.S.A

Social Profiles

Company Snapshot

Norwich Pharmaceuticals Inc. Discontinued

6826 NY-12, Norwich, NY 13815

U.S.A

www.norwichpharma.com/ info@norwichpharma.com View on Map
FDA Approved Drug Records ( 3 records )
1993
21 Apr
Discontinued Application: 20198

Drug Name

ADALAT CC

Product Number

1

Dosage Form

-

Strength

30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-04-21

20198 / 1

Active Ingredient

NIFEDIPINE

Application Number

20198

Product Number

1

Dosage Form

-

Strength

30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-04-21

Regulatory Status

Discontinued

1993
21 Apr
Discontinued Application: 20198

Drug Name

ADALAT CC

Product Number

2

Dosage Form

-

Strength

60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-04-21

20198 / 2

Active Ingredient

NIFEDIPINE

Application Number

20198

Product Number

2

Dosage Form

-

Strength

60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-04-21

Regulatory Status

Discontinued

1993
21 Apr
Discontinued Application: 20198

Drug Name

ADALAT CC

Product Number

3

Dosage Form

-

Strength

90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-04-21

20198 / 3

Active Ingredient

NIFEDIPINE

Application Number

20198

Product Number

3

Dosage Form

-

Strength

90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1993-04-21

Regulatory Status

Discontinued

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Drug Status Breakdown
3 total
  • Discontinued
Official Source

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

Drug Name

ADALAT CC

Application Number

20198

Product Number

1

Active Ingredient

NIFEDIPINE

Dosage Form

-

Strength

30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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