Abbott Laboratories Unclassified
FDA Approved Drugs

Abbott Laboratories Unclassified

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.

Unclassified
  • Total Records 4
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
176
View
Unclassified
4
View
Discontinued
172
View
Company Overview

Company

Abbott Laboratories Unclassified

Country

U.S.A

Website

Visit Website

Email

webmasterindia@abbott.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Abbott Laboratories Unclassified

100 Abbott Park Road, Abbott Park, IL 60064 - (224) 667-6100

U.S.A

www.abbott.com/ webmasterindia@abbott.com View on Map
FDA Approved Drug Records ( 4 records )
-
Unclassified Application: 20782

Drug Name

DEPAKOTE ER

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

20782 / 1

Active Ingredient

DIVALPROEX SODIUM

Application Number

20782

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 20782

Drug Name

DEPAKOTE ER

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

-

20782 / 2

Active Ingredient

DIVALPROEX SODIUM

Application Number

20782

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 13056

Drug Name

PENTHRANE

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

-

13056 / 1

Active Ingredient

METHOXYFLURANE

Application Number

13056

Product Number

1

Dosage Form

-

Strength

99.9%

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 12828

Drug Name

TRAVASE

Product Number

1

Dosage Form

-

Strength

82,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**

Approval Date

-

12828 / 1

Active Ingredient

SUTILAINS

Application Number

12828

Product Number

1

Dosage Form

-

Strength

82,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**

Approval Date

-

Regulatory Status

Unclassified

Related Databases
  • FDA Inspections
    249 View
  • EDQM CEP
    9 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    176 View
Drug Status Breakdown
4 total
  • Unclassified
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Drug Name

DEPAKOTE ER

Application Number

20782

Product Number

1

Active Ingredient

DIVALPROEX SODIUM

Dosage Form

-

Strength

250MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit