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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Serlin
Dosage Strength : 100mg
Packaging :
Approval Date : 11/03/2005
Application Number : 20040607006603
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Serlin
Dosage Strength : 50mg
Packaging :
Approval Date : 11/03/2005
Application Number : 20040607006597
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Sertrasen
Dosage Strength : 100mg
Packaging :
Approval Date : 11/03/2005
Application Number : 20040607011850
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Sertrasen
Dosage Strength : 50mg
Packaging :
Approval Date : 11/03/2005
Application Number : 20040607011843
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : CAMPRAL
Dosage Strength : 333MG **Federal Regist...
Packaging :
Approval Date : 2004-07-29
Application Number : 21431
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACARBOSE
Dosage Strength : 25MG
Packaging :
Approval Date : 2008-05-07
Application Number : 77532
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACARBOSE
Dosage Strength : 50MG
Packaging :
Approval Date : 2008-05-07
Application Number : 77532
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ACARBOSE
Dosage Strength : 100MG
Packaging :
Approval Date : 2008-05-07
Application Number : 77532
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Norway
Dosage Form : Infusion fluid, resoluti...
Brand Name : Acetaminophen Actavis
Dosage Strength : 10 mg/ml
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Infusion fluid, resoluti...
Brand Name : Acetaminophen Actavis
Dosage Strength : 10 mg/ml
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
RLD : Yes
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : CAMPRAL
Dosage Strength : 333MG **Federal Register...
Approval Date : 2004-07-29
Application Number : 21431
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ACARBOSE
Dosage Strength : 25MG
Approval Date : 2008-05-07
Application Number : 77532
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ACARBOSE
Dosage Strength : 50MG
Approval Date : 2008-05-07
Application Number : 77532
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ACARBOSE
Dosage Strength : 100MG
Approval Date : 2008-05-07
Application Number : 77532
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL AND ACETAMINO...
Dosage Strength : 325MG;50MG
Approval Date : 1984-10-19
Application Number : 87550
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : BANCAP
Dosage Strength : 325MG;50MG
Approval Date : 1986-01-16
Application Number : 88889
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL, ACETAMINOPHE...
Dosage Strength : 500MG;50MG;40MG
Approval Date : 1998-07-30
Application Number : 40267
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL, ACETAMINOPHE...
Dosage Strength : 325MG;50MG;40MG
Approval Date : 1984-11-09
Application Number : 88616
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AA
RLD : No
TE Code :
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL, ACETAMINOPHE...
Dosage Strength : 325MG;50MG;40MG
Approval Date : 1988-02-16
Application Number : 89536
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET; ORAL
Proprietary Name : ESGIC
Dosage Strength : 325MG;50MG;40MG
Approval Date : 1988-12-23
Application Number : 89660
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Excipients
REF. STANDARDS & IMPURITIES
Inspections and registrations
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Actavis Inc is a supplier offers 46 products (APIs, Excipients or Intermediates).
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