Dynapharm
FDA Approved Drugs

Dynapharm

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 1
  • Latest Approval Date Apr 20, 1988
  • Data Source FDA
  • First Approval Date Apr 20, 1988
Company Overview

Company

Dynapharm

Country

Malaysia

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Company Snapshot

Dynapharm

Lot 2497, Lorong Perusahaan Baru 5, Kawasan Perusahaan Perai 3, 13600 Perai, Pulau Pinang, Malaysia

Malaysia

dynapharm.com.my/ View on Map
FDA Approved Drug Records ( 1 record )
1988
20 Apr
Discontinued Application: 71320

Drug Name

COLOVAGE

Product Number

1

Dosage Form

-

Strength

227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET

Approval Date

1988-04-20

71320 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

Application Number

71320

Product Number

1

Dosage Form

-

Strength

227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET

Approval Date

1988-04-20

Regulatory Status

Discontinued

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Drug Status Breakdown
1 total
  • Discontinued
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

COLOVAGE

Application Number

71320

Product Number

1

Active Ingredient

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

Dosage Form

-

Strength

227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET

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