01 2ANI Pharmaceuticals Inc
02 6Actavis Inc
03 2Antibiotice SA
04 3Aurobindo Pharma Limited
05 2Baxter Healthcare Corporation
06 10Bristol Myers Squibb
07 6ELKINS SINN
08 3Fresenius Kabi USA
09 12GSK
10 2Hospira, Inc.
11 5Istituto Biochimico Italiano Giovanni Lorenzini SpA
12 3Piramal Enterprises Limited
13 2Reyoung pharmaceutical
14 2STERISCIENCE SPECLTS
15 3Sagent Pharmaceuticals
16 7Sandoz B2B
17 1Teva Pharmaceutical Industries
18 3Wockhardt
01 9CAPSULE;ORAL
02 4FOR SOLUTION;ORAL
03 55INJECTABLE;INJECTION
04 2POWDER;INTRAVENOUS
05 2Powder for Injection
06 2powder for injection /infusion
01 55DISCN
02 15RX
03 4Blank
01 12BACTOCILL
02 2BACTOCILL IN PLASTIC CONTAINER
03 1OXACILLIN Atb
04 1OXACILLIN Atb®
05 54OXACILLIN SODIUM
06 2PROSTAPHLIN
07 2Blank
01 2China
02 2Romania
03 70USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 62222
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 62222
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BACTOCILL IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Packaging :
Approval Date : 1989-10-26
Application Number : 50640
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BACTOCILL IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/ML
Packaging :
Approval Date : 1989-10-26
Application Number : 50640
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROSTAPHLIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50118
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROSTAPHLIN
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50194
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50195
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50195
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50195
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50195
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50195
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61450
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61450
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 61457
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-03-26
Application Number : 61334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-03-26
Application Number : 61334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-03-26
Application Number : 61334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-03-26
Application Number : 61334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 61334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61336
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61336
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 62241
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 62241
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BACTOCILL
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62321
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 61490
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 61490
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 61490
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 61490
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL
Packaging :
Approval Date : 1991-05-09
Application Number : 61490
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXACILLIN SODIUM
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62252
Regulatory Info : DISCN
Registration Country : USA
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