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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALENDRONATE SODIUM
Dosage Strength : EQ 10MG BASE
Approval Date : 2024-06-04
Application Number : 206387
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALENDRONATE SODIUM
Dosage Strength : EQ 35MG BASE
Approval Date : 2024-06-04
Application Number : 206387
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALENDRONATE SODIUM
Dosage Strength : EQ 40MG BASE
Approval Date : 2024-06-04
Application Number : 206387
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALENDRONATE SODIUM
Dosage Strength : EQ 70MG BASE
Approval Date : 2024-06-04
Application Number : 206387
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALLOPURINOL
Dosage Strength : 100MG
Approval Date : 2011-03-16
Application Number : 90637
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALLOPURINOL
Dosage Strength : 300MG
Approval Date : 2011-03-16
Application Number : 90637
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ATENOLOL
Dosage Strength : 25MG
Approval Date : 2006-12-27
Application Number : 77877
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ATENOLOL
Dosage Strength : 50MG
Approval Date : 2006-12-27
Application Number : 77877
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ATENOLOL
Dosage Strength : 100MG
Approval Date : 2006-12-27
Application Number : 77877
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG
Approval Date : 2014-03-11
Application Number : 202277
RX/OTC/DISCN : OTC
RLD : No
TE Code :
Regulatory Info : Generic CTD, BE
Registration Country : India
Dosage Form : TABLET
Brand Name : Zerodol
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic CTD, BE
Registration Country : India
Regulatory Info : Generic BE
Registration Country : India
Dosage Form : TABLET
Brand Name : Zerodol-CR
Dosage Strength : 200MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic BE
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : SYRUP
Brand Name :
Dosage Strength : 120MG/5ML
Packaging : 60 ML, 100 ML
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : SYRUP
Brand Name :
Dosage Strength : 125MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : TABLETS
Brand Name :
Dosage Strength : 500MG
Packaging : 10x10's, 100x10's,...
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : TABLETS
Brand Name :
Dosage Strength : 650MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : CHEWABLE TABLET
Brand Name : Nemozole
Dosage Strength : 400MG
Packaging :
Approval Date :
Application Number : 207844
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : FILM COATED TABLETS
Brand Name : Nemozole
Dosage Strength : 200MG
Packaging : 10x1x2's, 10x1x1's
Approval Date :
Application Number : 20666
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : FILM COATED TABLETS
Brand Name : Nemozole
Dosage Strength : 400MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Dosage Form : SUSPENSION
Brand Name : Nemozole
Dosage Strength : 100MG/5ML
Packaging : 20ML
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Inspections and registrations
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Ipca Laboratories is a supplier offers 154 products (APIs, Excipients or Intermediates).
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