DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories
02 1Amneal Pharmaceuticals
03 1Caplin Point Laboratories Limited
04 1Cipla
05 1Epic Pharma. LLC.
06 1Novartis Pharmaceuticals Corporation
07 1Sandoz B2B
01 1EMULSION
02 6EMULSION;OPHTHALMIC
01 5RX
02 2Blank
01 5DIFLUPREDNATE
02 2DUREZOL
01 1Canada
02 6USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : DIFLUPREDNATE
Dosage Form : EMULSION;OPHTHALMIC
Dosage Strength : 0.05%
Packaging :
Approval Date : 2022-11-16
Application Number : 214894
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DIFLUPREDNATE
Dosage Form : EMULSION;OPHTHALMIC
Dosage Strength : 0.05%
Packaging :
Approval Date : 2021-11-17
Application Number : 211526
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : DIFLUPREDNATE
Dosage Form : EMULSION;OPHTHALMIC
Dosage Strength : 0.05%
Packaging :
Approval Date :
Application Number : 219441
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DIFLUPREDNATE
Dosage Form : EMULSION;OPHTHALMIC
Dosage Strength : 0.05%
Packaging :
Approval Date : 2021-08-09
Application Number : 211776
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DIFLUPREDNATE
Dosage Form : EMULSION;OPHTHALMIC
Dosage Strength : 0.05%
Packaging :
Approval Date : 2024-05-14
Application Number : 207284
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Canada
Brand Name : DUREZOL
Dosage Form : EMULSION
Dosage Strength : 0.05%/W/V
Packaging : 5ML
Approval Date :
Application Number : 2415534
Regulatory Info :
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Brand Name : DUREZOL
Dosage Form : EMULSION;OPHTHALMIC
Dosage Strength : 0.05%
Packaging :
Approval Date : 2008-06-23
Application Number : 22212
Regulatory Info : RX
Registration Country : USA
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