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Approved Drug Products containing AM20060780 listed in the FDA Orange Book. Original Data : FDA Website

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01 2GRANULES

02 2ACCORD HLTHCARE

03 6ACTAVIS LABS FL INC

04 2ALEMBIC

05 2ANBISON LAB

06 3ANNORA PHARMA

07 2APNAR PHARMA LP

08 2APOTEX INC

09 7AUROBINDO PHARMA USA

10 2BAUSCH

11 2CADILA PHARMS LTD

12 6ENDO OPERATIONS

13 3EPIC PHARMA LLC

14 9GLAXOSMITHKLINE

15 2GRAVITI PHARMS

16 4HERITAGE PHARMA

17 6IMPAX LABS

18 7INVAGEN PHARMS

19 2INVATECH

20 6JUBILANT GENERICS

21 2LUPIN LTD

22 2MICRO LABS

23 1NALPROPION

24 3PRINSTON INC

25 1RISING PHARMA

26 4SANDOZ

27 6SCIEGEN PHARMS INC

28 2SINOTHERAPEUTICS INC

29 6SUN PHARM

30 3TORRENT

31 3TWI PHARMS

32 5WATSON LABS INC

33 5WOCKHARDT LTD

34 6YICHANG HUMANWELL

35 2ZHEJIANG JUTAI PHARM

36 2ZYDUS PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

RLD : No

TE Code : AB3

BUPROPION HYDROCHLORIDE

Brand Name : BUPROPION HYDROCHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 150MG

Approval Date : 2022-02-02

Application Number : 215568

RX/OTC/DISCN : RX

RLD : No

TE Code : AB3

Granules India

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

RLD : No

TE Code : AB3

BUPROPION HYDROCHLORIDE

Brand Name : BUPROPION HYDROCHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 300MG

Approval Date : 2022-02-02

Application Number : 215568

RX/OTC/DISCN : RX

RLD : No

TE Code : AB3

Granules India

03

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BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1985-12-30

Application Number : 18644

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

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BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN

Dosage Form : TABLET;ORAL

Dosage Strength : 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1985-12-30

Application Number : 18644

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

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BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1985-12-30

Application Number : 18644

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

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BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN SR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 50MG

Approval Date : 1996-10-04

Application Number : 20358

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

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BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN SR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 100MG

Approval Date : 1996-10-04

Application Number : 20358

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB1

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08

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BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN SR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 150MG

Approval Date : 1996-10-04

Application Number : 20358

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB1

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09

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BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN SR

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 200MG

Approval Date : 2002-06-14

Application Number : 20358

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB1

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10

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BUPROPION HYDROCHLORIDE

Brand Name : ZYBAN

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 100MG

Approval Date : 1997-05-14

Application Number : 20711

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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