Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 2TARO
02 4STRIDES PHARMA
03 1ABBOTT
04 4ABLE
05 2ABRAXIS PHARM
06 5ALEMBIC
07 2ALEMBIC PHARMS LTD
08 1AMNEAL
09 2AUROBINDO PHARMA LTD
10 2B BRAUN
11 2BAUSCH
12 1BAXTER HLTHCARE
13 1BAXTER HLTHCARE CORP
14 2CADILA
15 2CADILA PHARMS LTD
16 1CASPER PHARMA LLC
17 2CHARTWELL MOLECULES
18 2CHARTWELL RX
19 1CHEMO RESEARCH SL
20 4COSETTE
21 4ENCUBE
22 1ENDO OPERATIONS
23 2FLAMINGO PHARMS
24 4FOSUN PHARMA
25 3FOUGERA PHARMS
26 4GALDERMA LABS LP
27 1GLAND PHARMA LTD
28 1GLENMARK PHARMS LTD
29 2HALSEY
30 2HERITAGE PHARMS INC
31 1HIKMA
32 1HOSPIRA
33 1INFORLIFE
34 2INNOGENIX
35 1INTL MEDICATION
36 2IVAX SUB TEVA PHARMS
37 2LABS AF
38 1LABS JUVISE
39 1LNK
40 2LUPIN LTD
41 2MUTUAL PHARM
42 1NOSTRUM LABS INC
43 2ORTHO MCNEIL PHARM
44 1PADAGIS ISRAEL
45 6PFIZER
46 1PLIVA
47 1RICONPHARMA LLC
48 1RISING
49 1SAPTALIS PHARMS
50 2SAVAGE LABS
51 1SOLARIS PHARMA CORP
52 2SUPERPHARM
53 1TEVA PHARMS
54 1TEVA PHARMS USA
55 2UNICHEM
56 7WATSON LABS
57 1WATSON LABS INC
58 1ZYDUS LIFESCIENCES
01 7CAPSULE;ORAL
02 5CREAM;TOPICAL
03 10GEL;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 57TABLET;ORAL
01 50DISCN
02 65RX
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 79METRONIDAZOLE
17 1METRONIDAZOLE HYDROCHLORIDE
18 6METRONIDAZOLE IN PLASTIC CONTAINER
19 1NORITATE
20 1NUVESSA
21 2PROTOSTAT
22 1PYLERA
23 2SATRIC
24 1VANDAZOLE
01 98No
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 : AB
Brand Name : METRONIDAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Approval Date : 2016-05-25
Application Number : 208162
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : METRONIDAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 2016-05-25
Application Number : 208162
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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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