EMD Millipore Corporation Discontinued
FDA Approved Drugs
EMD Millipore Corporation Discontinued
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 22
- Latest Approval Date Apr 11, 2003
- Data Source FDA
- First Approval Date Mar 03, 1995
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EMD Millipore Corporation Discontinued
Burlington, Massachusetts 01803
U.S.A
www.emdmillipore.com/US/en View on MapFDA Approved Drug Records ( 22 records )
Drug Name
CETROTIDE
Product Number
2
Dosage Form
-
Strength
EQ 3MG BASE/VIAL
Approval Date
2000-08-11
Active Ingredient
CETRORELIX ACETATE
Application Number
21197
Product Number
2
Dosage Form
-
Strength
EQ 3MG BASE/VIAL
Approval Date
2000-08-11
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
1
Dosage Form
-
Strength
0.025MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
1
Dosage Form
-
Strength
0.025MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
2
Dosage Form
-
Strength
0.05MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
2
Dosage Form
-
Strength
0.05MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
3
Dosage Form
-
Strength
0.075MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
3
Dosage Form
-
Strength
0.075MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
4
Dosage Form
-
Strength
0.088MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
4
Dosage Form
-
Strength
0.088MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
5
Dosage Form
-
Strength
0.1MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
5
Dosage Form
-
Strength
0.1MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
6
Dosage Form
-
Strength
0.112MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
6
Dosage Form
-
Strength
0.112MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
7
Dosage Form
-
Strength
0.125MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
7
Dosage Form
-
Strength
0.125MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
8
Dosage Form
-
Strength
0.137MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
8
Dosage Form
-
Strength
0.137MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
9
Dosage Form
-
Strength
0.15MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
9
Dosage Form
-
Strength
0.15MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
10
Dosage Form
-
Strength
0.175MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
10
Dosage Form
-
Strength
0.175MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
11
Dosage Form
-
Strength
0.2MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
11
Dosage Form
-
Strength
0.2MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
EUTHYROX
Product Number
12
Dosage Form
-
Strength
0.3MG
Approval Date
2002-05-31
Active Ingredient
LEVOTHYROXINE SODIUM
Application Number
21292
Product Number
12
Dosage Form
-
Strength
0.3MG
Approval Date
2002-05-31
Regulatory Status
Discontinued
Drug Name
GEREF
Product Number
1
Dosage Form
-
Strength
EQ 0.5MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-09-26
Active Ingredient
SERMORELIN ACETATE
Application Number
20443
Product Number
1
Dosage Form
-
Strength
EQ 0.5MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-09-26
Regulatory Status
Discontinued
Drug Name
GEREF
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-09-26
Active Ingredient
SERMORELIN ACETATE
Application Number
20443
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-09-26
Regulatory Status
Discontinued
Drug Name
GLUCOPHAGE
Product Number
1
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-03-03
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
20357
Product Number
1
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-03-03
Regulatory Status
Discontinued
Drug Name
GLUCOPHAGE
Product Number
2
Dosage Form
-
Strength
850MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-03-03
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
20357
Product Number
2
Dosage Form
-
Strength
850MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-03-03
Regulatory Status
Discontinued
Drug Name
GLUCOPHAGE
Product Number
3
Dosage Form
-
Strength
625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-05
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
20357
Product Number
3
Dosage Form
-
Strength
625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-05
Regulatory Status
Discontinued
Drug Name
GLUCOPHAGE
Product Number
4
Dosage Form
-
Strength
750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-05
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
20357
Product Number
4
Dosage Form
-
Strength
750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-05
Regulatory Status
Discontinued
Drug Name
GLUCOPHAGE
Product Number
5
Dosage Form
-
Strength
1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-05
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
20357
Product Number
5
Dosage Form
-
Strength
1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-11-05
Regulatory Status
Discontinued
Drug Name
GLUCOPHAGE XR
Product Number
1
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-10-13
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
21202
Product Number
1
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2000-10-13
Regulatory Status
Discontinued
Drug Name
GLUCOPHAGE XR
Product Number
4
Dosage Form
-
Strength
750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-04-11
Active Ingredient
METFORMIN HYDROCHLORIDE
Application Number
21202
Product Number
4
Dosage Form
-
Strength
750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-04-11
Regulatory Status
Discontinued
Drug Status Breakdown
22 total- Discontinued
Official Source
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Drug Name
CETROTIDE
Application Number
21197
Product Number
2
Active Ingredient
CETRORELIX ACETATE
Dosage Form
-
Strength
EQ 3MG BASE/VIAL
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