VALIDUS PHARMS Discontinued
FDA Approved Drugs
VALIDUS PHARMS 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.
- Total Records 20
- Latest Approval Date Dec 11, 2001
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Snapshot
FDA Approved Drug Records ( 20 records )
Drug Name
ANZEMET
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1997-09-11
Active Ingredient
DOLASETRON MESYLATE
Application Number
20623
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1997-09-11
Regulatory Status
Discontinued
Drug Name
ANZEMET
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
1997-09-11
Active Ingredient
DOLASETRON MESYLATE
Application Number
20623
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
1997-09-11
Regulatory Status
Discontinued
Drug Name
ANZEMET
Product Number
1
Dosage Form
-
Strength
100MG/5ML (20MG/ML)
Approval Date
1997-09-11
Active Ingredient
DOLASETRON MESYLATE
Application Number
20624
Product Number
1
Dosage Form
-
Strength
100MG/5ML (20MG/ML)
Approval Date
1997-09-11
Regulatory Status
Discontinued
Drug Name
ANZEMET
Product Number
2
Dosage Form
-
Strength
12.5MG/0.625ML (20MG/ML)
Approval Date
1997-09-11
Active Ingredient
DOLASETRON MESYLATE
Application Number
20624
Product Number
2
Dosage Form
-
Strength
12.5MG/0.625ML (20MG/ML)
Approval Date
1997-09-11
Regulatory Status
Discontinued
Drug Name
ANZEMET
Product Number
3
Dosage Form
-
Strength
500MG/25ML (20MG/ML)
Approval Date
2001-12-11
Active Ingredient
DOLASETRON MESYLATE
Application Number
20624
Product Number
3
Dosage Form
-
Strength
500MG/25ML (20MG/ML)
Approval Date
2001-12-11
Regulatory Status
Discontinued
Drug Name
BUMEX
Product Number
1
Dosage Form
-
Strength
0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1983-02-28
Active Ingredient
BUMETANIDE
Application Number
18226
Product Number
1
Dosage Form
-
Strength
0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1983-02-28
Regulatory Status
Discontinued
Drug Name
LASIX
Product Number
1
Dosage Form
-
Strength
40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
FUROSEMIDE
Application Number
16273
Product Number
1
Dosage Form
-
Strength
40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LASIX
Product Number
2
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
FUROSEMIDE
Application Number
16273
Product Number
2
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LASIX
Product Number
3
Dosage Form
-
Strength
80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
FUROSEMIDE
Application Number
16273
Product Number
3
Dosage Form
-
Strength
80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LOPRESSOR HCT
Product Number
2
Dosage Form
-
Strength
25MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-12-31
Active Ingredient
HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE
Application Number
18303
Product Number
2
Dosage Form
-
Strength
25MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-12-31
Regulatory Status
Discontinued
Drug Name
LOPRESSOR HCT
Product Number
3
Dosage Form
-
Strength
50MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-12-31
Active Ingredient
HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE
Application Number
18303
Product Number
3
Dosage Form
-
Strength
50MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-12-31
Regulatory Status
Discontinued
Drug Name
LOTENSIN
Product Number
1
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-06-25
Active Ingredient
BENAZEPRIL HYDROCHLORIDE
Application Number
19851
Product Number
1
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-06-25
Regulatory Status
Discontinued
Drug Name
LOTENSIN HCT
Product Number
1
Dosage Form
-
Strength
5MG;6.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-05-19
Active Ingredient
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Application Number
20033
Product Number
1
Dosage Form
-
Strength
5MG;6.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-05-19
Regulatory Status
Discontinued
Drug Name
NORPRAMIN
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
14399
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NORPRAMIN
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
14399
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NORPRAMIN
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
1982-01-01
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
14399
Product Number
4
Dosage Form
-
Strength
75MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NORPRAMIN
Product Number
5
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
14399
Product Number
5
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NORPRAMIN
Product Number
6
Dosage Form
-
Strength
150MG
Approval Date
1982-01-01
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
14399
Product Number
6
Dosage Form
-
Strength
150MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NORPRAMIN
Product Number
7
Dosage Form
-
Strength
10MG
Approval Date
1982-02-11
Active Ingredient
DESIPRAMINE HYDROCHLORIDE
Application Number
14399
Product Number
7
Dosage Form
-
Strength
10MG
Approval Date
1982-02-11
Regulatory Status
Discontinued
Drug Name
TRENTAL
Product Number
1
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-08-30
Active Ingredient
PENTOXIFYLLINE
Application Number
18631
Product Number
1
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-08-30
Regulatory Status
Discontinued
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Drug Status Breakdown
20 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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Explore important FDA approved drug information available in the records above.
Drug Name
ANZEMET
Application Number
20623
Product Number
1
Active Ingredient
DOLASETRON MESYLATE
Dosage Form
-
Strength
50MG
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