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 2ENDO OPERATIONS
11 3EPIC PHARMA LLC
12 3ESJAY PHARMA
13 3HERITAGE
14 5NORVIUM BIOSCIENCE
15 2OXFORD PHARMS
16 6PFIZER
17 3RUBICON
18 5SUN PHARM INDS INC
19 3TEVA PHARMS
20 3UNIQUE
21 5WATSON LABS
22 2WATSON LABS TEVA
23 3ZYDUS PHARMS
24 3ZYDUS PHARMS USA INC
01 20TABLET, EXTENDED RELEASE;ORAL
02 53TABLET;ORAL
01 36DISCN
02 37RX
01 46GLIPIZIDE
02 18GLIPIZIDE AND METFORMIN HYDROCHLORIDE
03 3GLUCOTROL
04 3GLUCOTROL XL
05 3METAGLIP
01 64No
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Dosage Strength : 2.5MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
Brand Name : GLUCOTROL XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 5MG
Approval Date : 1994-04-26
Application Number : 20329
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 : 10MG
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 : 2.5MG
Approval Date : 1999-08-10
Application Number : 20329
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
