Bristol Laboratories Ltd Discontinued
FDA Approved Drugs
Bristol Laboratories Ltd 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 61
- Latest Approval Date Sep 06, 1996
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
Bristol Laboratories Ltd Discontinued
Country
United Kingdom
Website
Social Profiles
Company Snapshot
Bristol Laboratories Ltd Discontinued
Bristol House, Unit 3, Canalside, Northbridge Road Berkhamsted, Hertfordshire
United Kingdom
bristol-labs.co.uk/ info@bristol-labs.co.uk View on MapFDA Approved Drug Records ( 61 records )
Drug Name
BETAPEN-VK
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Active Ingredient
PENICILLIN V POTASSIUM
Application Number
61150
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BETAPEN-VK
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Active Ingredient
PENICILLIN V POTASSIUM
Application Number
61150
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRISTACYCLINE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE HYDROCHLORIDE
Application Number
61658
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRISTACYCLINE
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE HYDROCHLORIDE
Application Number
61658
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRISTACYCLINE
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE HYDROCHLORIDE
Application Number
61888
Product Number
1
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRISTACYCLINE
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE HYDROCHLORIDE
Application Number
61888
Product Number
2
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRISTAGEN
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1982-01-01
Active Ingredient
GENTAMICIN SULFATE
Application Number
62288
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRISTAMYCIN
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Active Ingredient
ERYTHROMYCIN STEARATE
Application Number
61304
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRISTAMYCIN
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Active Ingredient
ERYTHROMYCIN STEARATE
Application Number
61887
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1984-05-07
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62464
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1984-05-07
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
1984-05-07
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62464
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
1984-05-07
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM
Product Number
3
Dosage Form
-
Strength
EQ 4GM BASE/VIAL
Approval Date
1984-05-07
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62464
Product Number
3
Dosage Form
-
Strength
EQ 4GM BASE/VIAL
Approval Date
1984-05-07
Regulatory Status
Discontinued
Drug Name
MEXATE
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
METHOTREXATE SODIUM
Application Number
86358
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MEXATE
Product Number
2
Dosage Form
-
Strength
EQ 50MG BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
METHOTREXATE SODIUM
Application Number
86358
Product Number
2
Dosage Form
-
Strength
EQ 50MG BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MEXATE
Product Number
3
Dosage Form
-
Strength
EQ 100MG BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
METHOTREXATE SODIUM
Application Number
86358
Product Number
3
Dosage Form
-
Strength
EQ 100MG BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MEXATE
Product Number
4
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
METHOTREXATE SODIUM
Application Number
86358
Product Number
4
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MUTAMYCIN
Product Number
1
Dosage Form
-
Strength
5MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
MITOMYCIN
Application Number
50450
Product Number
1
Dosage Form
-
Strength
5MG/VIAL **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
MUTAMYCIN
Product Number
2
Dosage Form
-
Strength
20MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
MITOMYCIN
Application Number
50450
Product Number
2
Dosage Form
-
Strength
20MG/VIAL **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
POLYCILLIN
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE
Application Number
50093
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POLYCILLIN
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE
Application Number
50308
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POLYCILLIN
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE
Application Number
50308
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POLYCILLIN
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE
Application Number
50308
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POLYCILLIN
Product Number
4
Dosage Form
-
Strength
EQ 100MG BASE/ML
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE
Application Number
50308
Product Number
4
Dosage Form
-
Strength
EQ 100MG BASE/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POLYCILLIN
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE
Application Number
50310
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POLYCILLIN
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE
Application Number
50310
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POLYCILLIN-N
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN SODIUM
Application Number
50309
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/VIAL **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
POLYCILLIN-N
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN SODIUM
Application Number
50309
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/VIAL **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
POLYCILLIN-N
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN SODIUM
Application Number
50309
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/VIAL **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
POLYCILLIN-N
Product Number
4
Dosage Form
-
Strength
EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN SODIUM
Application Number
50309
Product Number
4
Dosage Form
-
Strength
EQ 1GM BASE/VIAL **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
POLYCILLIN-N
Product Number
5
Dosage Form
-
Strength
EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN SODIUM
Application Number
50309
Product Number
5
Dosage Form
-
Strength
EQ 2GM BASE/VIAL **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
POLYCILLIN-PRB
Product Number
1
Dosage Form
-
Strength
EQ 3.5GM BASE/BOT;1GM/BOT
Approval Date
1982-01-01
Active Ingredient
AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID
Application Number
50457
Product Number
1
Dosage Form
-
Strength
EQ 3.5GM BASE/BOT;1GM/BOT
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PRECEF
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
1984-05-24
Active Ingredient
CEFORANIDE
Application Number
50554
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
1984-05-24
Regulatory Status
Discontinued
Drug Name
PRECEF
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1984-05-24
Active Ingredient
CEFORANIDE
Application Number
50554
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1984-05-24
Regulatory Status
Discontinued
Drug Name
PRECEF
Product Number
3
Dosage Form
-
Strength
2GM/VIAL
Approval Date
1984-05-24
Active Ingredient
CEFORANIDE
Application Number
50554
Product Number
3
Dosage Form
-
Strength
2GM/VIAL
Approval Date
1984-05-24
Regulatory Status
Discontinued
Drug Name
PRECEF
Product Number
4
Dosage Form
-
Strength
10GM/VIAL
Approval Date
1984-05-24
Active Ingredient
CEFORANIDE
Application Number
50554
Product Number
4
Dosage Form
-
Strength
10GM/VIAL
Approval Date
1984-05-24
Regulatory Status
Discontinued
Drug Name
PRECEF
Product Number
5
Dosage Form
-
Strength
20GM/VIAL
Approval Date
1984-05-24
Active Ingredient
CEFORANIDE
Application Number
50554
Product Number
5
Dosage Form
-
Strength
20GM/VIAL
Approval Date
1984-05-24
Regulatory Status
Discontinued
Drug Name
TETREX
Product Number
2
Dosage Form
-
Strength
EQ 250MG HYDROCHLORIDE
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE PHOSPHATE COMPLEX
Application Number
50212
Product Number
2
Dosage Form
-
Strength
EQ 250MG HYDROCHLORIDE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETREX
Product Number
3
Dosage Form
-
Strength
EQ 500MG HYDROCHLORIDE
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE PHOSPHATE COMPLEX
Application Number
50212
Product Number
3
Dosage Form
-
Strength
EQ 500MG HYDROCHLORIDE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETREX
Product Number
1
Dosage Form
-
Strength
EQ 100MG HYDROCHLORIDE
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE PHOSPHATE COMPLEX
Application Number
61653
Product Number
1
Dosage Form
-
Strength
EQ 100MG HYDROCHLORIDE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETREX
Product Number
2
Dosage Form
-
Strength
EQ 250MG HYDROCHLORIDE
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE PHOSPHATE COMPLEX
Application Number
61653
Product Number
2
Dosage Form
-
Strength
EQ 250MG HYDROCHLORIDE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETREX
Product Number
3
Dosage Form
-
Strength
EQ 500MG HYDROCHLORIDE
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE PHOSPHATE COMPLEX
Application Number
61653
Product Number
3
Dosage Form
-
Strength
EQ 500MG HYDROCHLORIDE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETREX
Product Number
1
Dosage Form
-
Strength
EQ 500MG HYDROCHLORIDE
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE PHOSPHATE COMPLEX
Application Number
61889
Product Number
1
Dosage Form
-
Strength
EQ 500MG HYDROCHLORIDE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TETREX
Product Number
2
Dosage Form
-
Strength
EQ 250MG HYDROCHLORIDE
Approval Date
1982-01-01
Active Ingredient
TETRACYCLINE PHOSPHATE COMPLEX
Application Number
61889
Product Number
2
Dosage Form
-
Strength
EQ 250MG HYDROCHLORIDE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ULTRACEF
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1982-03-16
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62376
Product Number
1
Dosage Form
-
Strength
EQ 125MG BASE/5ML
Approval Date
1982-03-16
Regulatory Status
Discontinued
Drug Name
ULTRACEF
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1982-03-16
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62376
Product Number
2
Dosage Form
-
Strength
EQ 250MG BASE/5ML
Approval Date
1982-03-16
Regulatory Status
Discontinued
Drug Name
ULTRACEF
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
1982-03-16
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62376
Product Number
3
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
1982-03-16
Regulatory Status
Discontinued
Drug Name
ULTRACEF
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-03-16
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62378
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE
Approval Date
1982-03-16
Regulatory Status
Discontinued
Drug Name
ULTRACEF
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
1982-08-31
Active Ingredient
CEFADROXIL/CEFADROXIL HEMIHYDRATE
Application Number
62408
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
1982-08-31
Regulatory Status
Discontinued
Drug Name
VERSAPEN
Product Number
1
Dosage Form
-
Strength
EQ 112.5MG AMPICIL/5ML
Approval Date
1982-01-01
Active Ingredient
HETACILLIN
Application Number
50060
Product Number
1
Dosage Form
-
Strength
EQ 112.5MG AMPICIL/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VERSAPEN
Product Number
3
Dosage Form
-
Strength
EQ 112.5MG AMPICIL/ML
Approval Date
1982-01-01
Active Ingredient
HETACILLIN
Application Number
50060
Product Number
3
Dosage Form
-
Strength
EQ 112.5MG AMPICIL/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VERSAPEN
Product Number
1
Dosage Form
-
Strength
EQ 112.5MG AMPICIL/ML
Approval Date
1982-01-01
Active Ingredient
HETACILLIN
Application Number
61398
Product Number
1
Dosage Form
-
Strength
EQ 112.5MG AMPICIL/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VERSAPEN
Product Number
2
Dosage Form
-
Strength
EQ 225MG AMPICIL/5ML
Approval Date
1982-01-01
Active Ingredient
HETACILLIN
Application Number
61398
Product Number
2
Dosage Form
-
Strength
EQ 225MG AMPICIL/5ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VERSAPEN-K
Product Number
1
Dosage Form
-
Strength
EQ 225MG AMPICIL
Approval Date
1982-01-01
Active Ingredient
HETACILLIN POTASSIUM
Application Number
61396
Product Number
1
Dosage Form
-
Strength
EQ 225MG AMPICIL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VERSAPEN-K
Product Number
2
Dosage Form
-
Strength
EQ 450MG AMPICIL
Approval Date
1982-01-01
Active Ingredient
HETACILLIN POTASSIUM
Application Number
61396
Product Number
2
Dosage Form
-
Strength
EQ 450MG AMPICIL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VIDEX
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1991-10-09
Active Ingredient
DIDANOSINE
Application Number
20156
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1991-10-09
Regulatory Status
Discontinued
Drug Name
ZERIT
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1994-06-24
Active Ingredient
STAVUDINE
Application Number
20412
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1994-06-24
Regulatory Status
Discontinued
Drug Name
ZERIT
Product Number
2
Dosage Form
-
Strength
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Active Ingredient
STAVUDINE
Application Number
20412
Product Number
2
Dosage Form
-
Strength
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Regulatory Status
Discontinued
Drug Name
ZERIT
Product Number
3
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Active Ingredient
STAVUDINE
Application Number
20412
Product Number
3
Dosage Form
-
Strength
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Regulatory Status
Discontinued
Drug Name
ZERIT
Product Number
4
Dosage Form
-
Strength
30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Active Ingredient
STAVUDINE
Application Number
20412
Product Number
4
Dosage Form
-
Strength
30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Regulatory Status
Discontinued
Drug Name
ZERIT
Product Number
5
Dosage Form
-
Strength
40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Active Ingredient
STAVUDINE
Application Number
20412
Product Number
5
Dosage Form
-
Strength
40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1994-06-24
Regulatory Status
Discontinued
Drug Name
ZERIT
Product Number
1
Dosage Form
-
Strength
1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-09-06
Active Ingredient
STAVUDINE
Application Number
20413
Product Number
1
Dosage Form
-
Strength
1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-09-06
Regulatory Status
Discontinued
Drug Status Breakdown
61 total- Discontinued
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Drug Name
BETAPEN-VK
Application Number
61150
Product Number
1
Active Ingredient
PENICILLIN V POTASSIUM
Dosage Form
-
Strength
EQ 250MG BASE
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