01 2AJANTA PHARMA LTD
02 2ALKEM LABS LTD
03 3ANI PHARMS
04 2APOTEX
05 2AUROBINDO PHARMA LTD
06 2CHARTWELL MOLECULAR
07 1DEXCEL
08 2DR REDDYS
09 3DR REDDYS LABS LTD
10 1GLENMARK PHARMS
11 2HETERO LABS LTD III
12 2INVENTIA
13 2KRKA TOVARNA ZDRAVIL
14 1LANNETT CO INC
15 2MACLEODS PHARMS LTD
16 3MYLAN
17 2MYLAN PHARMS INC
18 1NATCO
19 2NATCO PHARMA LTD
20 2NOVITIUM PHARMA
21 1PERRIGO PHARMA INTL
22 1PERRIGO R AND D
23 1RISING
24 3SANDOZ
25 2SUN PHARM
26 6TAKEDA PHARMS NA
27 5TAKEDA PHARMS USA
28 2TEVA PHARMS
29 2TEVA PHARMS USA
30 2XIROMED
31 2ZYDUS HLTHCARE
32 2ZYDUS PHARMS
01 3CAPSULE, DELAYED REL PELLETS, TABLET;ORAL
02 43CAPSULE, DELAYED REL PELLETS;ORAL
03 4CAPSULE, TABLET, CAPSULE, DELAYED REL PELLETS;ORAL
04 2FOR SUSPENSION, DELAYED RELEASE;ORAL
05 1INJECTABLE;INTRAVENOUS
06 15TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE;ORAL
01 25DISCN
02 6OTC
03 37RX
01 53LANSOPRAZOLE
02 3LANSOPRAZOLE, AMOXICILLIN AND CLARITHROMYCIN (COPACKAGED)
03 6PREVACID
04 1PREVACID 24 HR
05 1PREVACID IV
06 1PREVACID NAPRAPAC 250 (COPACKAGED)
07 1PREVACID NAPRAPAC 375 (COPACKAGED)
08 1PREVACID NAPRAPAC 500 (COPACKAGED)
09 1PREVPAC (COPACKAGED)
01 60No
02 8Yes
RLD : Yes
TE Code :
Brand Name : PREVACID
Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL
Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1995-05-10
Application Number : 20406
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : PREVACID
Dosage Form : CAPSULE, DELAYED REL PELLETS;ORAL
Dosage Strength : 30MG
Approval Date : 1995-05-10
Application Number : 20406
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
Brand Name : PREVACID
Dosage Form : FOR SUSPENSION, DELAYED RELEASE;ORAL
Dosage Strength : 15MG/PACKET
Approval Date : 2001-05-03
Application Number : 21281
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PREVACID
Dosage Form : FOR SUSPENSION, DELAYED RELEASE;ORAL
Dosage Strength : 30MG/PACKET
Approval Date : 2001-05-03
Application Number : 21281
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AB
Brand Name : PREVACID
Dosage Form : TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE;ORAL
Dosage Strength : 15MG
Approval Date : 2002-08-30
Application Number : 21428
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : PREVACID
Dosage Form : TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE;ORAL
Dosage Strength : 30MG
Approval Date : 2002-08-30
Application Number : 21428
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : PREVACID NAPRAPAC 250 (COPACKAGED)
Dosage Form : CAPSULE, DELAYED REL PELLETS, TABLET;ORAL
Dosage Strength : 15MG,N/A;N/A,250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2003-11-14
Application Number : 21507
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : PREVACID NAPRAPAC 375 (COPACKAGED)
Dosage Form : CAPSULE, DELAYED REL PELLETS, TABLET;ORAL
Dosage Strength : 15MG,N/A;N/A,375MG
Approval Date : 2003-11-14
Application Number : 21507
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PREVACID NAPRAPAC 500 (COPACKAGED)
Dosage Form : CAPSULE, DELAYED REL PELLETS, TABLET;ORAL
Dosage Strength : 15MG,N/A;N/A,500MG
Approval Date : 2003-11-14
Application Number : 21507
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : PREVACID IV
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : 30MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2004-05-27
Application Number : 21566
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
