01 2ACCORD HLTHCARE
02 4ANI PHARMS
03 2APOTEX
04 3AUROBINDO PHARMA
05 2AUROBINDO PHARMA USA
06 2BARR LABS INC
07 3BRISTOL MYERS SQUIBB
08 2CHARTWELL RX
09 2ENDO OPERATIONS
10 3EPIC PHARMA LLC
11 3ESJAY PHARMA
12 3HERITAGE
13 5NORVIUM BIOSCIENCE
14 2OXFORD PHARMS
15 6PFIZER
16 3RUBICON
17 2SANDOZ
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 35DISCN
02 38RX
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Dosage Strength : 2.5MG;250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 2.5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 5MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 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 : 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
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