Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 2TARO
02 2STRIDES PHARMA
03 1ABBOTT
04 4ABLE
05 2ABRAXIS PHARM
06 1AILEX PHARMS LLC
07 5ALEMBIC
08 2ALEMBIC PHARMS LTD
09 1AMNEAL
10 2APPCO
11 3AUROBINDO PHARMA LTD
12 2B BRAUN
13 2BAUSCH
14 1BAXTER HLTHCARE
15 1BAXTER HLTHCARE CORP
16 2CADILA
17 2CADILA PHARMS LTD
18 1CASPER PHARMA LLC
19 2CHARTWELL MOLECULES
20 2CHARTWELL RX
21 1CHEMO RESEARCH SL
22 4COSETTE
23 4ENCUBE
24 1ENDO OPERATIONS
25 2ESJAY PHARMA
26 2FLAMINGO PHARMS
27 4FOSUN PHARMA
28 3FOUGERA PHARMS
29 4GALDERMA LABS LP
30 1GLAND PHARMA LTD
31 1GLENMARK PHARMS LTD
32 2HALSEY
33 1HIKMA
34 1HOSPIRA
35 1INFORLIFE
36 3INNOGENIX
37 1INTL MEDICATION
38 2IVAX SUB TEVA PHARMS
39 2LABS AF
40 1LABS JUVISE
41 1LNK
42 2LUPIN LTD
43 2MUTUAL PHARM
44 1NOVAST LABS
45 2ORTHO MCNEIL PHARM
46 1PADAGIS ISRAEL
47 6PFIZER
48 1PLIVA
49 1RISING
50 1SAPTALIS PHARMS
51 2SAVAGE LABS
52 1SOLARIS PHARMA CORP
53 2SUPERPHARM
54 1TEVA PHARMS
55 1TEVA PHARMS USA
56 2UNICHEM
57 7WATSON LABS
58 1WATSON LABS INC
59 1ZYDUS LIFESCIENCES
01 7CAPSULE;ORAL
02 5CREAM;TOPICAL
03 11GEL;TOPICAL
04 10GEL;VAGINAL
05 18INJECTABLE;INJECTION
06 2LOTION;TOPICAL
07 1SUSPENSION;ORAL
08 2TABLET, CHEWABLE, TABLET, CAPSULE;ORAL
09 3TABLET, EXTENDED RELEASE;ORAL
10 58TABLET;ORAL
01 50DISCN
02 67RX
01 2BISMUTH SUBCITRATE POTASSIUM, METRONIDAZOLE AND TETRACYCLINE HYDROCHLORIDE
02 1BISMUTH SUBSALICYLATE, METRONIDAZOLE AND TETRACYCLINE HYDROCHLORIDE
03 3FLAGYL
04 1FLAGYL ER
05 1FLAGYL I.V.
06 2FLAGYL I.V. RTU IN PLASTIC CONTAINER
07 1HELIDAC
08 1LIKMEZ
09 1METRO I.V.
10 1METRO I.V. IN PLASTIC CONTAINER
11 1METROCREAM
12 2METROGEL
13 1METROGEL-VAGINAL
14 1METROLOTION
15 2METROMIDOL
16 81METRONIDAZOLE
17 1METRONIDAZOLE HYDROCHLORIDE
18 6METRONIDAZOLE IN PLASTIC CONTAINER
19 1NORITATE
20 1NUVESSA
21 2PROTOSTAT
22 1PYLERA
23 2SATRIC
24 1VANDAZOLE
01 100No
02 17Yes
RLD : No
TE Code : AB
Brand Name : METRONIDAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 1985-01-29
Application Number : 70039
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : METRONIDAZOLE
Dosage Form : GEL;TOPICAL
Dosage Strength : 0.75%
Approval Date : 2006-07-18
Application Number : 77819
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : METRONIDAZOLE
Dosage Form : GEL;TOPICAL
Dosage Strength : 1%
Approval Date : 2017-03-14
Application Number : 204651
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : METRONIDAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Approval Date : 1985-01-29
Application Number : 70040
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : METRONIDAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Approval Date : 1982-01-01
Application Number : 18517
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : METRONIDAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 1982-05-05
Application Number : 18517
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : FLAGYL
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12623
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : FLAGYL
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12623
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : FLAGYL I.V.
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18353
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : FLAGYL I.V. RTU IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 500MG/100ML
Approval Date : 1982-01-01
Application Number : 18353
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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