Interpharm
FDA Approved Drugs
Interpharm
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.
- Total Records 17
- Latest Approval Date Sep 02, 1988
- Data Source FDA
- First Approval Date Sep 23, 1986
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Interpharm
Palestine, Gaza Strip, Tal-Elhawa, 8 St
Egypt
www.interpharm.ps/ info@interpharm.ps View on MapFDA Approved Drug Records ( 17 records )
Drug Name
CLONIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.1MG
Approval Date
1986-10-01
Active Ingredient
CLONIDINE HYDROCHLORIDE
Application Number
71252
Product Number
1
Dosage Form
-
Strength
0.1MG
Approval Date
1986-10-01
Regulatory Status
Discontinued
Drug Name
CLONIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.2MG
Approval Date
1986-10-01
Active Ingredient
CLONIDINE HYDROCHLORIDE
Application Number
71253
Product Number
1
Dosage Form
-
Strength
0.2MG
Approval Date
1986-10-01
Regulatory Status
Discontinued
Drug Name
CLONIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.3MG
Approval Date
1986-10-01
Active Ingredient
CLONIDINE HYDROCHLORIDE
Application Number
71254
Product Number
1
Dosage Form
-
Strength
0.3MG
Approval Date
1986-10-01
Regulatory Status
Discontinued
Drug Name
DISOPYRAMIDE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1987-01-15
Active Ingredient
DISOPYRAMIDE PHOSPHATE
Application Number
71190
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1987-01-15
Regulatory Status
Discontinued
Drug Name
DISOPYRAMIDE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1987-01-15
Active Ingredient
DISOPYRAMIDE PHOSPHATE
Application Number
71191
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1987-01-15
Regulatory Status
Discontinued
Drug Name
DOXYCYCLINE HYCLATE
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1988-09-02
Active Ingredient
DOXYCYCLINE HYCLATE
Application Number
62763
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1988-09-02
Regulatory Status
Discontinued
Drug Name
DOXYCYCLINE HYCLATE
Product Number
2
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1988-09-02
Active Ingredient
DOXYCYCLINE HYCLATE
Application Number
62763
Product Number
2
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1988-09-02
Regulatory Status
Discontinued
Drug Name
DOXYCYCLINE HYCLATE
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1988-09-02
Active Ingredient
DOXYCYCLINE HYCLATE
Application Number
62764
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1988-09-02
Regulatory Status
Discontinued
Drug Name
METOCLOPRAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
1986-09-24
Active Ingredient
METOCLOPRAMIDE HYDROCHLORIDE
Application Number
71213
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
1986-09-24
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1987-05-05
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71368
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1987-05-05
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1987-05-05
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71369
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1987-05-05
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1987-05-05
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71370
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1987-05-05
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
1987-05-05
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71371
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
1987-05-05
Regulatory Status
Discontinued
Drug Name
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Product Number
1
Dosage Form
-
Strength
400MG;80MG
Approval Date
1987-10-27
Active Ingredient
SULFAMETHOXAZOLE; TRIMETHOPRIM
Application Number
71299
Product Number
1
Dosage Form
-
Strength
400MG;80MG
Approval Date
1987-10-27
Regulatory Status
Discontinued
Drug Name
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Product Number
1
Dosage Form
-
Strength
800MG;160MG
Approval Date
1987-10-27
Active Ingredient
SULFAMETHOXAZOLE; TRIMETHOPRIM
Application Number
71300
Product Number
1
Dosage Form
-
Strength
800MG;160MG
Approval Date
1987-10-27
Regulatory Status
Discontinued
Drug Name
TOLAZAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1986-09-23
Active Ingredient
TOLAZAMIDE
Application Number
71270
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1986-09-23
Regulatory Status
Discontinued
Drug Name
TOLAZAMIDE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1986-09-23
Active Ingredient
TOLAZAMIDE
Application Number
71271
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1986-09-23
Regulatory Status
Discontinued
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Drug Status Breakdown
17 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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Drug Name
CLONIDINE HYDROCHLORIDE
Application Number
71252
Product Number
1
Active Ingredient
CLONIDINE HYDROCHLORIDE
Dosage Form
-
Strength
0.1MG
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