Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 2STRIDES PHARMA
02 1ANI PHARMS
03 3APOTEX INC
04 23APOTHECON
05 6AUROBINDO
06 2AUROBINDO PHARMA
07 10AUROBINDO PHARMA LTD
08 2CHARTWELL
09 8CHARTWELL RX
10 2CIPLA
11 1CUMBERLAND
12 5DEVA HOLDING AS
13 2ENDO OPERATIONS
14 6GLAXOSMITHKLINE
15 7HIKMA
16 6HIKMA PHARMS
17 2LABS ATRAL
18 3MICRO LABS
19 5MICRO LABS LTD INDIA
20 4MYLAN
21 4PARKE DAVIS
22 2PHATHOM
23 1PRAGMA
24 3RANBAXY LABS LTD
25 1REDHILL
26 1RISING
27 15SANDOZ
28 5SANDOZ INC
29 17SUN PHARM INDS LTD
30 1TAKEDA PHARMS USA
31 25TEVA
32 1TEVA PHARMS USA
33 29US ANTIBIOTICS
34 4WYETH AYERST
01 1CAPSULE, DELAYED RELEASE;ORAL
02 4CAPSULE, TABLET, CAPSULE, DELAYED REL PELLETS;ORAL
03 1CAPSULE, TABLET, CAPSULE, DELAYED RELEASE;ORAL
04 1CAPSULE, TABLET, TABLET;ORAL
05 1CAPSULE, TABLET;ORAL
06 1CAPSULE; ORAL
07 40CAPSULE;ORAL
08 88FOR SUSPENSION;ORAL
09 28TABLET, CHEWABLE;ORAL
10 3TABLET, EXTENDED RELEASE;ORAL
11 5TABLET, FOR SUSPENSION;ORAL
12 36TABLET;ORAL
01 110DISCN
02 98RX
03 1Blank
01 77AMOXICILLIN
02 55AMOXICILLIN AND CLAVULANATE POTASSIUM
03 1AMOXICILLIN PEDIATRIC
04 19AMOXIL
05 2AUGMENTIN 125
06 2AUGMENTIN 200
07 3AUGMENTIN 250
08 2AUGMENTIN 400
09 1AUGMENTIN 500
10 1AUGMENTIN 875
11 1AUGMENTIN ES-600
12 1AUGMENTIN XR
13 3DISPERMOX
14 3LANSOPRAZOLE, AMOXICILLIN AND CLARITHROMYCIN (COPACKAGED)
15 3LAROTID
16 1MOXATAG
17 1OMECLAMOX-PAK
18 4POLYMOX
19 1PREVPAC (COPACKAGED)
20 1TALICIA
21 17TRIMOX
22 4UTIMOX
23 1VOQUEZNA DUAL PAK
24 1VOQUEZNA TRIPLE PAK
25 4WYMOX
01 177No
02 31Yes
03 1Blank
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code :
Brand Name : AMOXICILLIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : 500MG
Approval Date : 1988-02-25
Application Number : 62881
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
RLD : No
TE Code :
Brand Name : AMOXICILLIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : 250MG
Approval Date : 1988-02-25
Application Number : 62884
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : AMOXIL
Dosage Form : CAPSULE;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Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50459
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : AMOXIL
Dosage Form : CAPSULE;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 : 50459
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : AMOXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50460
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : AMOXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : 250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50460
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : AMOXIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50460
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LAROTID
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50460
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : AMOXIL
Dosage Form : TABLET, CHEWABLE;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 : 50542
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : AMOXIL
Dosage Form : TABLET, CHEWABLE;ORAL
Dosage Strength : 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50542
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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