01 2ACCORD HLTHCARE
02 2AIPING PHARM INC
03 4ANI PHARMS
04 2APOTEX
05 3AUROBINDO PHARMA
06 2AUROBINDO PHARMA USA
07 2BARR LABS INC
08 3BRISTOL MYERS SQUIBB
09 2CHARTWELL RX
10 2DIFGEN PHARMS
11 3EPIC PHARMA LLC
12 2GRAVITI PHARMS
13 3HERITAGE
14 3NOVITIUM PHARMA
15 2OXFORD PHARMS
16 6PFIZER
17 2PH HEALTH
18 5PHARMOBEDIENT
19 4RUBICON RESEARCH
20 5SUN PHARM INDS INC
21 3TEVA PHARMS
22 3UNIQUE
23 6WATSON LABS
24 2WATSON LABS TEVA
25 2YUNG SHIN PHARM
26 3ZYDUS PHARMS
27 3ZYDUS PHARMS USA INC
01 2SYSTEM;TRANSDERMAL
02 20TABLET, EXTENDED RELEASE;ORAL
03 59TABLET;ORAL
01 37DISCN
02 44RX
01 2CLONIDINE
02 2CLONIDINE HYDROCHLORIDE
03 49GLIPIZIDE
04 18GLIPIZIDE AND METFORMIN HYDROCHLORIDE
05 3GLUCOTROL
06 3GLUCOTROL XL
07 3METAGLIP
08 1PINDOLOL
01 72No
02 9Yes
RLD : No
TE Code : AB
Brand Name : GLIPIZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 1995-02-27
Application Number : 74223
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
GLIPIZIDE; METFORMIN HYDROCHLORIDE
Brand Name : METAGLIP
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2002-10-21
Application Number : 21460
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
GLIPIZIDE; METFORMIN HYDROCHLORIDE
Brand Name : METAGLIP
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2002-10-21
Application Number : 21460
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
GLIPIZIDE; METFORMIN HYDROCHLORIDE
Brand Name : METAGLIP
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2002-10-21
Application Number : 21460
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : GLUCOTROL
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1984-05-08
Application Number : 17783
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : GLUCOTROL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1984-05-08
Application Number : 17783
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : GLUCOTROL
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1993-05-11
Application Number : 17783
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : GLUCOTROL XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 5MG
Approval Date : 1994-04-26
Application Number : 20329
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : GLUCOTROL XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 10MG
Approval Date : 1994-04-26
Application Number : 20329
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : GLUCOTROL XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 2.5MG
Approval Date : 1999-08-10
Application Number : 20329
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
