Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 2STRIDES PHARMA
02 1ABBOTT
03 4ABLE
04 2ABRAXIS PHARM
05 1AILEX PHARMS LLC
06 5ALEMBIC
07 2ALEMBIC PHARMS LTD
08 1AMNEAL
09 2APPCO
10 3AUROBINDO PHARMA LTD
11 2B BRAUN
12 2BAUSCH
13 1BAXTER HLTHCARE
14 1BAXTER HLTHCARE CORP
15 2CADILA
16 2CADILA PHARMS LTD
17 1CASPER PHARMA LLC
18 2CHARTWELL MOLECULES
19 2CHARTWELL RX
20 1CHEMO RESEARCH SL
21 4COSETTE
22 4ENCUBE
23 1ENDO OPERATIONS
24 2ESJAY PHARMA
25 2FLAMINGO PHARMS
26 4FOSUN PHARMA
27 3FOUGERA PHARMS
28 4GALDERMA LABS LP
29 1GLAND PHARMA LTD
30 1GLENMARK PHARMS LTD
31 2HALSEY
32 1HIKMA
33 1HOSPIRA
34 1INFORLIFE
35 3INNOGENIX
36 1INTL MEDICATION
37 2IVAX SUB TEVA PHARMS
38 2LABS AF
39 1LABS JUVISE
40 1LNK
41 2LUPIN LTD
42 2MUTUAL PHARM
43 1NOVAST LABS
44 2ORTHO MCNEIL PHARM
45 1PADAGIS ISRAEL
46 6PFIZER
47 1PLIVA
48 1RISING
49 1SAPTALIS PHARMS
50 2SAVAGE LABS
51 1SOLARIS PHARMA CORP
52 2SUPERPHARM
53 2TARO
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 : 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 : 1982-09-17
Application Number : 18599
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : METRONIDAZOLE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 1984-02-13
Application Number : 18599
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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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