BEDFORD LABS Discontinued
FDA Approved Drugs
BEDFORD LABS 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 53
- Latest Approval Date Aug 18, 2008
- Data Source FDA
- First Approval Date Feb 16, 1982
Company Overview
Social Profiles
Company Snapshot
BEDFORD LABS Discontinued
300 Northfield Road Bedford, OH 44146 U.S.A.
U.S.A
www.bedfordlabs.com/ View on MapFDA Approved Drug Records ( 53 records )
Drug Name
AMIODARONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
2002-10-15
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
76018
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
2002-10-15
Regulatory Status
Discontinued
Drug Name
AMIODARONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
2002-10-15
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
76088
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
2002-10-15
Regulatory Status
Discontinued
Drug Name
AMIODARONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
2002-10-24
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
76299
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
2002-10-24
Regulatory Status
Discontinued
Drug Name
CEFAZOLIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
1988-07-21
Active Ingredient
CEFAZOLIN SODIUM
Application Number
62894
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
1988-07-21
Regulatory Status
Discontinued
Drug Name
CEFAZOLIN SODIUM
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
1988-07-21
Active Ingredient
CEFAZOLIN SODIUM
Application Number
62894
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
1988-07-21
Regulatory Status
Discontinued
Drug Name
CEFAZOLIN SODIUM
Product Number
3
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1988-07-21
Active Ingredient
CEFAZOLIN SODIUM
Application Number
62894
Product Number
3
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1988-07-21
Regulatory Status
Discontinued
Drug Name
CEFAZOLIN SODIUM
Product Number
4
Dosage Form
-
Strength
EQ 5GM BASE/VIAL
Approval Date
1988-07-21
Active Ingredient
CEFAZOLIN SODIUM
Application Number
62894
Product Number
4
Dosage Form
-
Strength
EQ 5GM BASE/VIAL
Approval Date
1988-07-21
Regulatory Status
Discontinued
Drug Name
CEFAZOLIN SODIUM
Product Number
5
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
1988-07-21
Active Ingredient
CEFAZOLIN SODIUM
Application Number
62894
Product Number
5
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
1988-07-21
Regulatory Status
Discontinued
Drug Name
CEFTRIAXONE
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
2008-08-18
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65465
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
2008-08-18
Regulatory Status
Discontinued
Drug Name
CEFTRIAXONE
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2008-08-18
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65465
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2008-08-18
Regulatory Status
Discontinued
Drug Name
CEFTRIAXONE
Product Number
3
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-08-18
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65465
Product Number
3
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-08-18
Regulatory Status
Discontinued
Drug Name
CEFTRIAXONE
Product Number
4
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2008-08-18
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65465
Product Number
4
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2008-08-18
Regulatory Status
Discontinued
Drug Name
CEFTRIAXONE
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2008-08-18
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65475
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2008-08-18
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN
Product Number
1
Dosage Form
-
Strength
200MG/20ML (10MG/ML)
Approval Date
2006-08-28
Active Ingredient
CIPROFLOXACIN
Application Number
76992
Product Number
1
Dosage Form
-
Strength
200MG/20ML (10MG/ML)
Approval Date
2006-08-28
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN
Product Number
2
Dosage Form
-
Strength
400MG/40ML (10MG/ML)
Approval Date
2006-08-28
Active Ingredient
CIPROFLOXACIN
Application Number
76992
Product Number
2
Dosage Form
-
Strength
400MG/40ML (10MG/ML)
Approval Date
2006-08-28
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN
Product Number
1
Dosage Form
-
Strength
1200MG/120ML (10MG/ML)
Approval Date
2006-08-28
Active Ingredient
CIPROFLOXACIN
Application Number
76993
Product Number
1
Dosage Form
-
Strength
1200MG/120ML (10MG/ML)
Approval Date
2006-08-28
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
2008-03-18
Active Ingredient
CIPROFLOXACIN
Application Number
78114
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
2008-03-18
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
400MG/200ML
Approval Date
2008-03-18
Active Ingredient
CIPROFLOXACIN
Application Number
78114
Product Number
2
Dosage Form
-
Strength
400MG/200ML
Approval Date
2008-03-18
Regulatory Status
Discontinued
Drug Name
CISPLATIN
Product Number
1
Dosage Form
-
Strength
10MG/VIAL
Approval Date
2000-11-14
Active Ingredient
CISPLATIN
Application Number
74713
Product Number
1
Dosage Form
-
Strength
10MG/VIAL
Approval Date
2000-11-14
Regulatory Status
Discontinued
Drug Name
CISPLATIN
Product Number
2
Dosage Form
-
Strength
50MG/VIAL
Approval Date
2000-11-14
Active Ingredient
CISPLATIN
Application Number
74713
Product Number
2
Dosage Form
-
Strength
50MG/VIAL
Approval Date
2000-11-14
Regulatory Status
Discontinued
Drug Name
CLINDAMYCIN PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE/ML
Approval Date
1994-06-30
Active Ingredient
CLINDAMYCIN PHOSPHATE
Application Number
63163
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE/ML
Approval Date
1994-06-30
Regulatory Status
Discontinued
Drug Name
DESMOPRESSIN ACETATE
Product Number
1
Dosage Form
-
Strength
0.004MG/ML
Approval Date
2000-02-18
Active Ingredient
DESMOPRESSIN ACETATE
Application Number
74575
Product Number
1
Dosage Form
-
Strength
0.004MG/ML
Approval Date
2000-02-18
Regulatory Status
Discontinued
Drug Name
DESMOPRESSIN ACETATE PRESERVATIVE FREE
Product Number
1
Dosage Form
-
Strength
0.004MG/ML
Approval Date
2000-02-18
Active Ingredient
DESMOPRESSIN ACETATE
Application Number
74574
Product Number
1
Dosage Form
-
Strength
0.004MG/ML
Approval Date
2000-02-18
Regulatory Status
Discontinued
Drug Name
FLUOROURACIL
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1988-01-26
Active Ingredient
FLUOROURACIL
Application Number
89508
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1988-01-26
Regulatory Status
Discontinued
Drug Name
FOLIC ACID
Product Number
1
Dosage Form
-
Strength
5MG/ML
Approval Date
1993-12-29
Active Ingredient
FOLIC ACID
Application Number
81066
Product Number
1
Dosage Form
-
Strength
5MG/ML
Approval Date
1993-12-29
Regulatory Status
Discontinued
Drug Name
KETOROLAC TROMETHAMINE
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1999-10-25
Active Ingredient
KETOROLAC TROMETHAMINE
Application Number
75230
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
1999-10-25
Regulatory Status
Discontinued
Drug Name
KETOROLAC TROMETHAMINE
Product Number
2
Dosage Form
-
Strength
15MG/ML
Approval Date
1999-10-25
Active Ingredient
KETOROLAC TROMETHAMINE
Application Number
75230
Product Number
2
Dosage Form
-
Strength
15MG/ML
Approval Date
1999-10-25
Regulatory Status
Discontinued
Drug Name
LORAZEPAM
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2005-07-13
Active Ingredient
LORAZEPAM
Application Number
77076
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2005-07-13
Regulatory Status
Discontinued
Drug Name
LORAZEPAM
Product Number
2
Dosage Form
-
Strength
4MG/ML
Approval Date
2005-07-13
Active Ingredient
LORAZEPAM
Application Number
77076
Product Number
2
Dosage Form
-
Strength
4MG/ML
Approval Date
2005-07-13
Regulatory Status
Discontinued
Drug Name
LORAZEPAM PRESERVATIVE FREE
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2005-07-13
Active Ingredient
LORAZEPAM
Application Number
77074
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2005-07-13
Regulatory Status
Discontinued
Drug Name
LORAZEPAM PRESERVATIVE FREE
Product Number
2
Dosage Form
-
Strength
4MG/ML
Approval Date
2005-07-13
Active Ingredient
LORAZEPAM
Application Number
77074
Product Number
2
Dosage Form
-
Strength
4MG/ML
Approval Date
2005-07-13
Regulatory Status
Discontinued
Drug Name
METHYLPREDNISOLONE SODIUM SUCCINATE
Product Number
2
Dosage Form
-
Strength
EQ 125MG BASE/VIAL
Approval Date
2007-02-21
Active Ingredient
METHYLPREDNISOLONE SODIUM SUCCINATE
Application Number
40641
Product Number
2
Dosage Form
-
Strength
EQ 125MG BASE/VIAL
Approval Date
2007-02-21
Regulatory Status
Discontinued
Drug Name
METHYLPREDNISOLONE SODIUM SUCCINATE
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2007-02-21
Active Ingredient
METHYLPREDNISOLONE SODIUM SUCCINATE
Application Number
40641
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2007-02-21
Regulatory Status
Discontinued
Drug Name
METHYLPREDNISOLONE SODIUM SUCCINATE
Product Number
4
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2007-02-21
Active Ingredient
METHYLPREDNISOLONE SODIUM SUCCINATE
Application Number
40641
Product Number
4
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2007-02-21
Regulatory Status
Discontinued
Drug Name
METHYLPREDNISOLONE SODIUM SUCCINATE
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE/VIAL
Approval Date
2007-02-21
Active Ingredient
METHYLPREDNISOLONE SODIUM SUCCINATE
Application Number
40662
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE/VIAL
Approval Date
2007-02-21
Regulatory Status
Discontinued
Drug Name
METHYLPREDNISOLONE SODIUM SUCCINATE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2007-02-21
Active Ingredient
METHYLPREDNISOLONE SODIUM SUCCINATE
Application Number
40709
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2007-02-21
Regulatory Status
Discontinued
Drug Name
METHYLPREDNISOLONE SODIUM SUCCINATE
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2007-02-21
Active Ingredient
METHYLPREDNISOLONE SODIUM SUCCINATE
Application Number
40709
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2007-02-21
Regulatory Status
Discontinued
Drug Name
METOCLOPRAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1992-03-30
Active Ingredient
METOCLOPRAMIDE HYDROCHLORIDE
Application Number
72155
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1992-03-30
Regulatory Status
Discontinued
Drug Name
METOCLOPRAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1992-03-30
Active Ingredient
METOCLOPRAMIDE HYDROCHLORIDE
Application Number
72244
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1992-03-30
Regulatory Status
Discontinued
Drug Name
METOCLOPRAMIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1992-05-18
Active Ingredient
METOCLOPRAMIDE HYDROCHLORIDE
Application Number
72247
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1992-05-18
Regulatory Status
Discontinued
Drug Name
MIDAZOLAM HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-06-23
Active Ingredient
MIDAZOLAM HYDROCHLORIDE
Application Number
75249
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-06-23
Regulatory Status
Discontinued
Drug Name
MIDAZOLAM HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-06-20
Active Ingredient
MIDAZOLAM HYDROCHLORIDE
Application Number
75455
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-06-20
Regulatory Status
Discontinued
Drug Name
NEOSAR
Product Number
1
Dosage Form
-
Strength
100MG/VIAL
Approval Date
1982-02-16
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
87442
Product Number
1
Dosage Form
-
Strength
100MG/VIAL
Approval Date
1982-02-16
Regulatory Status
Discontinued
Drug Name
NEOSAR
Product Number
2
Dosage Form
-
Strength
200MG/VIAL
Approval Date
1982-02-16
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
87442
Product Number
2
Dosage Form
-
Strength
200MG/VIAL
Approval Date
1982-02-16
Regulatory Status
Discontinued
Drug Name
NEOSAR
Product Number
3
Dosage Form
-
Strength
500MG/VIAL
Approval Date
1982-02-16
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
87442
Product Number
3
Dosage Form
-
Strength
500MG/VIAL
Approval Date
1982-02-16
Regulatory Status
Discontinued
Drug Name
NEOSAR
Product Number
4
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1983-07-08
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
87442
Product Number
4
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1983-07-08
Regulatory Status
Discontinued
Drug Name
NEOSAR
Product Number
5
Dosage Form
-
Strength
2GM/VIAL
Approval Date
1989-03-30
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
87442
Product Number
5
Dosage Form
-
Strength
2GM/VIAL
Approval Date
1989-03-30
Regulatory Status
Discontinued
Drug Name
OFLOXACIN
Product Number
1
Dosage Form
-
Strength
40MG/ML
Approval Date
2002-01-16
Active Ingredient
OFLOXACIN
Application Number
75762
Product Number
1
Dosage Form
-
Strength
40MG/ML
Approval Date
2002-01-16
Regulatory Status
Discontinued
Drug Name
PROMETHAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
2004-03-17
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
40524
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
2004-03-17
Regulatory Status
Discontinued
Drug Name
PROMETHAZINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
50MG/ML
Approval Date
2004-03-17
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
40524
Product Number
2
Dosage Form
-
Strength
50MG/ML
Approval Date
2004-03-17
Regulatory Status
Discontinued
Drug Name
RANITIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE/ML
Approval Date
2004-11-19
Active Ingredient
RANITIDINE HYDROCHLORIDE
Application Number
74764
Product Number
1
Dosage Form
-
Strength
EQ 25MG BASE/ML
Approval Date
2004-11-19
Regulatory Status
Discontinued
Drug Name
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Product Number
1
Dosage Form
-
Strength
80MG/ML;16MG/ML
Approval Date
1992-04-29
Active Ingredient
SULFAMETHOXAZOLE; TRIMETHOPRIM
Application Number
72383
Product Number
1
Dosage Form
-
Strength
80MG/ML;16MG/ML
Approval Date
1992-04-29
Regulatory Status
Discontinued
Drug Name
VERAPAMIL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
1995-07-28
Active Ingredient
VERAPAMIL HYDROCHLORIDE
Application Number
72888
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
1995-07-28
Regulatory Status
Discontinued
Drug Status Breakdown
53 total- Discontinued
Official Source
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Drug Name
AMIODARONE HYDROCHLORIDE
Application Number
76018
Product Number
1
Active Ingredient
AMIODARONE HYDROCHLORIDE
Dosage Form
-
Strength
50MG/ML
FDA Approved Drug Data
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