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Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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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 3BEXIMCO PHARMS USA
09 4CHARTWELL RX
10 3DR REDDYS LABS LTD
11 2EPI HLTH
12 3IMPAX LABS
13 3IMPAX LABS INC
14 7JOURNEY
15 1LEDERLE
16 1NEXUS PHARMS
17 3NORVIUM BIOSCIENCE
18 1ORAPHARMA
19 1REMPEX
20 5RISING PHARMA
21 8SANDOZ
22 7SUN PHARM
23 3SUN PHARM INDS INC
24 8SUN PHARM INDS LTD
25 3SUN PHARM INDUSTRIES
26 6TORRENT
27 4TRIAX PHARMS
28 2WATSON LABS
29 1WATSON LABS TEVA
30 3ZYDUS
31 8ZYDUS PHARMS
01 2AEROSOL, FOAM;TOPICAL
02 5CAPSULE, EXTENDED RELEASE;ORAL
03 26CAPSULE;ORAL
04 2INJECTABLE;INJECTION
05 1POWDER, EXTENDED RELEASE;DENTAL
06 1SUSPENSION;ORAL
07 3TABLET, EXTENDED RELEASE; ORAL
08 74TABLET, EXTENDED RELEASE;ORAL
09 20TABLET;ORAL
10 2Tablet, Extended Release; Oral
11 1VIAL; SINGLE-USE
01 61DISCN
02 69RX
03 7Blank
01 1AMZEEQ
02 1ARESTIN
03 3DYNACIN
04 8MINOCIN
05 1MINOCYCLINE
06 107MINOCYCLINE HYDROCHLORIDE
07 2MINOLIRA
08 8SOLODYN
09 5XIMINO
10 1ZILXI
01 113No
02 17Yes
03 7Blank
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code : AB
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: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code : AB
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: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code : AB
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
RLD : No
TE Code :
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 :
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code :
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 :
RLD : No
TE Code :
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 :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code :
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 :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : Yes
TE Code :
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 :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : Yes
TE Code :
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 :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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