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01 3STRIDES PHARMA

02 8ALKEM LABS LTD

03 3ALVOGEN

04 3AUROBINDO PHARMA

05 11AUROBINDO PHARMA LTD

06 7BARR LABS INC

07 12BAUSCH

08 7CHARTWELL RX

09 2EPI HLTH

10 3IMPAX LABS

11 3IMPAX LABS INC

12 8JOURNEY

13 1LEDERLE

14 1NEXUS

15 1ORAPHARMA

16 3PHARMOBEDIENT

17 3REGCON HOLDINGS

18 1REMPEX

19 5RISING

20 8SANDOZ

21 7SUN PHARM

22 3SUN PHARM INDS INC

23 8SUN PHARM INDS LTD

24 3SUN PHARM INDUSTRIES

25 6TORRENT

26 4TRIAX PHARMS

27 2WATSON LABS

28 1WATSON LABS TEVA

29 3ZYDUS

30 8ZYDUS PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

RLD : No

TE Code : AB

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCYCLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 50MG BASE

Approval Date : 2003-04-16

Application Number : 65131

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

RLD : No

TE Code : AB

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCYCLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 75MG BASE

Approval Date : 2003-04-16

Application Number : 65131

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

RLD : No

TE Code : AB

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCYCLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Approval Date : 2003-04-16

Application Number : 65131

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

04

AIChE Annual Meeting
Not Confirmed
arrow
arrow
AIChE Annual Meeting
Not Confirmed

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : EQ 50MG BASE/5ML

Approval Date : 1982-01-01

Application Number : 50445

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

AIChE Annual Meeting
Not Confirmed
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arrow
AIChE Annual Meeting
Not Confirmed

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Approval Date : 1990-05-31

Application Number : 50649

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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06

REMPEX

U.S.A
AIChE Annual Meeting
Not Confirmed
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REMPEX

U.S.A
arrow
AIChE Annual Meeting
Not Confirmed

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 100MG BASE/VIAL

Approval Date : 1982-01-01

Application Number : 50444

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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07

TRIAX PHARMS

Country
AIChE Annual Meeting
Not Confirmed
arrow

TRIAX PHARMS

Country
arrow
AIChE Annual Meeting
Not Confirmed

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 100MG BASE

Approval Date : 1982-01-01

Application Number : 50315

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

08

TRIAX PHARMS

Country
AIChE Annual Meeting
Not Confirmed
arrow

TRIAX PHARMS

Country
arrow
AIChE Annual Meeting
Not Confirmed

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 50MG BASE

Approval Date : 1982-01-01

Application Number : 50315

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

09

TRIAX PHARMS

Country
AIChE Annual Meeting
Not Confirmed
arrow

TRIAX PHARMS

Country
arrow
AIChE Annual Meeting
Not Confirmed

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCYCLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

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

Approval Date : 1982-08-10

Application Number : 50451

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

TRIAX PHARMS

Country
AIChE Annual Meeting
Not Confirmed
arrow

TRIAX PHARMS

Country
arrow
AIChE Annual Meeting
Not Confirmed

MINOCYCLINE HYDROCHLORIDE

Brand Name : MINOCYCLINE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

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

Approval Date : 1982-08-10

Application Number : 50451

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank