DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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01 4Dr. Reddy's Laboratories
02 2AAIPharma Services Corp.
03 4ANI Pharmaceuticals Inc
04 2Arrow Pharmaceuticals
05 4Aurobindo Pharma Limited
06 1Brilliant LifeSciences
07 2Eli Lilly
08 9H. Lundbeck AS
09 1Lucent Biotech Ltd
10 5Mallinckrodt Pharmaceuticals
11 2Medreich
12 1PHARM ASSOC
13 2Pharmascience Inc.
14 2Pluviaendo
15 4Pulse Pharmaceuticals
16 1RELIANCE FORMULATION PVT. LTD
17 2RIVOPHARM SA
18 1Rekah Pharmaceutical
19 4Ria Generics
20 4Rising Pharmaceuticals Inc
21 1Rubicon Research
22 1Sun Pharmaceutical Industries Limited
23 5Taro Pharmaceutical Industries
24 8Teva Pharmaceutical Industries
25 4Zydus Lifesciences
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01 3Antic-calc Tablet, Film Coated
02 4CAPSULE
03 38CAPSULE;ORAL
04 1Capsule
05 6Film Coated Tablet
06 1Nortriptyline 10Mg 30 Joined' Oral Use
07 1Nortriptyline 25Mg 30 Joined' Oral Use
08 5SOLUTION;ORAL
09 13Tablet
10 2tablet
11 2Blank
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01 2Allowed
02 1Approved
03 29DISCN
04 3Deregistered
05 2Prescription
06 14RX
07 25Blank
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01 3AVENTYL
02 2AVENTYL HYDROCHLORIDE
03 2Allegron
04 1Doloneuron NT 400
05 1Doloneuron-NT 100
06 1Doloneuron-NT 200
07 1Dominans
08 35NORTRIPTYLINE HYDROCHLORIDE
09 1NORTYLIN
10 5Noritren
11 2Nortriptyline Ria
12 2Nortriptyline Rivopharm
13 1Notar
14 5PAMELOR
15 2PMS-NORTRIPTYLINE
16 1Prenura NT
17 1SENSARIL
18 2Sensa Selection
19 1Strong Dominans
20 7Blank
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01 2Australia
02 4Canada
03 9India
04 1Israel
05 4Italy
06 3Norway
07 4Sweden
08 2Switzerland
09 2Turkey
10 43USA
11 2Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 1992-03-30
Application Number : 73556
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1992-03-30
Application Number : 73556
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1992-03-30
Application Number : 73556
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 1992-03-30
Application Number : 73556
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1992-12-31
Application Number : 74054
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1992-12-31
Application Number : 74054
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 1992-12-31
Application Number : 74054
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 1992-12-31
Application Number : 74054
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AVENTYL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 14684
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AVENTYL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 14684
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PAMELOR
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 10MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 18012
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PAMELOR
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 18013
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PAMELOR
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 18013
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PAMELOR
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 18013
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PAMELOR
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 18013
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AVENTYL
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14685
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 1996-04-11
Application Number : 73667
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 1996-04-11
Application Number : 73667
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 1996-04-11
Application Number : 73667
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORTRIPTYLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 1996-04-11
Application Number : 73667
Regulatory Info : DISCN
Registration Country : USA