DAVA PHARMS INC
FDA Approved Drugs
DAVA PHARMS INC
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 47
- Latest Approval Date Jan 28, 2000
- Data Source FDA
- First Approval Date Jan 01, 1982
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FDA Approved Drug Records ( 47 records )
Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
1996-09-20
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Application Number
40098
Product Number
1
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
Approval Date
1996-09-20
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1996-02-13
Active Ingredient
CAPTOPRIL
Application Number
74423
Product Number
1
Dosage Form
-
Strength
12.5MG
Approval Date
1996-02-13
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1996-02-13
Active Ingredient
CAPTOPRIL
Application Number
74423
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1996-02-13
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1996-02-13
Active Ingredient
CAPTOPRIL
Application Number
74423
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
1996-02-13
Regulatory Status
Discontinued
Drug Name
CAPTOPRIL
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
1996-02-13
Active Ingredient
CAPTOPRIL
Application Number
74423
Product Number
4
Dosage Form
-
Strength
100MG
Approval Date
1996-02-13
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1995-04-27
Active Ingredient
CEFACLOR
Application Number
64107
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1995-04-27
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1995-04-27
Active Ingredient
CEFACLOR
Application Number
64107
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1995-04-27
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 375MG BASE/5ML
Approval Date
1995-04-28
Active Ingredient
CEFACLOR
Application Number
64110
Product Number
1
Dosage Form
-
Strength
EQ 375MG BASE/5ML
Approval Date
1995-04-28
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1995-04-28
Active Ingredient
CEFACLOR
Application Number
64114
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1995-04-28
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 187MG BASE/5ML
Approval Date
1995-04-28
Active Ingredient
CEFACLOR
Application Number
64115
Product Number
1
Dosage Form
-
Strength
EQ 187MG BASE/5ML
Approval Date
1995-04-28
Regulatory Status
Discontinued
Drug Name
CEFACLOR
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1995-04-28
Active Ingredient
CEFACLOR
Application Number
64116
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1995-04-28
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1987-09-04
Active Ingredient
CHLORPROPAMIDE
Application Number
89561
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1987-09-04
Regulatory Status
Discontinued
Drug Name
CHLORPROPAMIDE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1987-09-04
Active Ingredient
CHLORPROPAMIDE
Application Number
89562
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1987-09-04
Regulatory Status
Discontinued
Drug Name
CHLORTHALIDONE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Active Ingredient
CHLORTHALIDONE
Application Number
87450
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORTHALIDONE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
CHLORTHALIDONE
Application Number
87451
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CLORAZEPATE DIPOTASSIUM
Product Number
1
Dosage Form
-
Strength
3.75MG
Approval Date
1987-12-14
Active Ingredient
CLORAZEPATE DIPOTASSIUM
Application Number
71742
Product Number
1
Dosage Form
-
Strength
3.75MG
Approval Date
1987-12-14
Regulatory Status
Discontinued
Drug Name
CLORAZEPATE DIPOTASSIUM
Product Number
1
Dosage Form
-
Strength
7.5MG
Approval Date
1987-12-14
Active Ingredient
CLORAZEPATE DIPOTASSIUM
Application Number
71743
Product Number
1
Dosage Form
-
Strength
7.5MG
Approval Date
1987-12-14
Regulatory Status
Discontinued
Drug Name
CLORAZEPATE DIPOTASSIUM
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
1987-12-14
Active Ingredient
CLORAZEPATE DIPOTASSIUM
Application Number
71744
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
1987-12-14
Regulatory Status
Discontinued
Drug Name
DIAZEPAM
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Active Ingredient
DIAZEPAM
Application Number
70226
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DIAZEPAM
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
DIAZEPAM
Application Number
70227
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1988-01-05
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
71673
Product Number
1
Dosage Form
-
Strength
EQ 50MG BASE
Approval Date
1988-01-05
Regulatory Status
Discontinued
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
1988-01-05
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
71674
Product Number
1
Dosage Form
-
Strength
EQ 75MG BASE
Approval Date
1988-01-05
Regulatory Status
Discontinued
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1988-01-05
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
71675
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE
Approval Date
1988-01-05
Regulatory Status
Discontinued
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1988-01-05
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
71676
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE
Approval Date
1988-01-05
Regulatory Status
Discontinued
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
1988-01-05
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
71685
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE
Approval Date
1988-01-05
Regulatory Status
Discontinued
Drug Name
DOXEPIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
1988-01-05
Active Ingredient
DOXEPIN HYDROCHLORIDE
Application Number
71686
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE
Approval Date
1988-01-05
Regulatory Status
Discontinued
Drug Name
FENOPROFEN CALCIUM
Product Number
1
Dosage Form
-
Strength
EQ 600MG BASE
Approval Date
1988-08-17
Active Ingredient
FENOPROFEN CALCIUM
Application Number
72326
Product Number
1
Dosage Form
-
Strength
EQ 600MG BASE
Approval Date
1988-08-17
Regulatory Status
Discontinued
Drug Name
HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE
Application Number
87060
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METHYLDOPA AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
15MG;250MG
Approval Date
1989-06-02
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
72507
Product Number
1
Dosage Form
-
Strength
15MG;250MG
Approval Date
1989-06-02
Regulatory Status
Discontinued
Drug Name
METHYLDOPA AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
25MG;250MG
Approval Date
1989-06-02
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
72508
Product Number
1
Dosage Form
-
Strength
25MG;250MG
Approval Date
1989-06-02
Regulatory Status
Discontinued
Drug Name
METHYLDOPA AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
30MG;500MG
Approval Date
1989-06-02
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
72509
Product Number
1
Dosage Form
-
Strength
30MG;500MG
Approval Date
1989-06-02
Regulatory Status
Discontinued
Drug Name
METHYLDOPA AND HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
50MG;500MG
Approval Date
1989-06-02
Active Ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Application Number
72510
Product Number
1
Dosage Form
-
Strength
50MG;500MG
Approval Date
1989-06-02
Regulatory Status
Discontinued
Drug Name
MORPHINE SULFATE
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
2000-01-28
Active Ingredient
MORPHINE SULFATE
Application Number
75407
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
2000-01-28
Regulatory Status
RX
Drug Name
NAPROXEN
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1993-12-21
Active Ingredient
NAPROXEN
Application Number
74105
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1993-12-21
Regulatory Status
Discontinued
Drug Name
NAPROXEN
Product Number
2
Dosage Form
-
Strength
375MG
Approval Date
1993-12-21
Active Ingredient
NAPROXEN
Application Number
74105
Product Number
2
Dosage Form
-
Strength
375MG
Approval Date
1993-12-21
Regulatory Status
Discontinued
Drug Name
NAPROXEN
Product Number
3
Dosage Form
-
Strength
500MG
Approval Date
1993-12-21
Active Ingredient
NAPROXEN
Application Number
74105
Product Number
3
Dosage Form
-
Strength
500MG
Approval Date
1993-12-21
Regulatory Status
Discontinued
Drug Name
PRAZOSIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
1989-05-16
Active Ingredient
PRAZOSIN HYDROCHLORIDE
Application Number
72705
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
1989-05-16
Regulatory Status
Discontinued
Drug Name
PRAZOSIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
1989-05-16
Active Ingredient
PRAZOSIN HYDROCHLORIDE
Application Number
72706
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
1989-05-16
Regulatory Status
Discontinued
Drug Name
PRAZOSIN HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
1989-05-16
Active Ingredient
PRAZOSIN HYDROCHLORIDE
Application Number
72707
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE
Approval Date
1989-05-16
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1985-07-30
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
70125
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1985-07-30
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1985-07-30
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
70126
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
1985-07-30
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1985-07-30
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
70127
Product Number
1
Dosage Form
-
Strength
40MG
Approval Date
1985-07-30
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
1985-07-30
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
70128
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
1985-07-30
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
1987-12-31
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71495
Product Number
1
Dosage Form
-
Strength
60MG
Approval Date
1987-12-31
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
90MG
Approval Date
1987-12-31
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
71496
Product Number
1
Dosage Form
-
Strength
90MG
Approval Date
1987-12-31
Regulatory Status
Discontinued
Drug Name
QUINIDINE SULFATE
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Active Ingredient
QUINIDINE SULFATE
Application Number
87011
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TOLBUTAMIDE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
TOLBUTAMIDE
Application Number
86926
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
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Drug Status Breakdown
47 total- Discontinued
- Unclassified
- RX
Official Source
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Drug Name
ACETAMINOPHEN AND CODEINE PHOSPHATE
Application Number
40098
Product Number
1
Active Ingredient
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form
-
Strength
120MG/5ML;12MG/5ML
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