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 3EPIC PHARMA LLC
11 2GRAVITI PHARMS
12 3HERITAGE
13 3NOVITIUM PHARMA
14 2OXFORD PHARMS
15 6PFIZER
16 2PH HEALTH
17 5PHARMOBEDIENT
18 4RUBICON RESEARCH
19 5SUN PHARM INDS INC
20 3TEVA PHARMS
21 3UNIQUE
22 5WATSON LABS
23 2WATSON LABS TEVA
24 3ZYDUS PHARMS
25 3ZYDUS PHARMS USA INC
01 20TABLET, EXTENDED RELEASE;ORAL
02 56TABLET;ORAL
01 34DISCN
02 42RX
01 49GLIPIZIDE
02 18GLIPIZIDE AND METFORMIN HYDROCHLORIDE
03 3GLUCOTROL
04 3GLUCOTROL XL
05 3METAGLIP
01 67No
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Dosage Strength : 2.5MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
