Takeda Pharmaceutical Discontinued
FDA Approved Drugs
Takeda Pharmaceutical 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 31
- Latest Approval Date Sep 15, 2021
- Data Source FDA
- First Approval Date Dec 30, 1988
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Takeda Pharmaceutical Discontinued
1-1, Nihonbashi-Honcho 2-chome, Chuo-ku, Tokyo 103-8668
Japan
www.takeda.com/ View on MapFDA Approved Drug Records ( 31 records )
Drug Name
ACTOPLUS MET
Product Number
1
Dosage Form
-
Strength
500MG;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-08-29
Active Ingredient
METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Application Number
21842
Product Number
1
Dosage Form
-
Strength
500MG;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2005-08-29
Regulatory Status
Discontinued
Drug Name
ACTOPLUS MET XR
Product Number
1
Dosage Form
-
Strength
1GM;EQ 15MG BASE
Approval Date
2009-05-12
Active Ingredient
METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Application Number
22024
Product Number
1
Dosage Form
-
Strength
1GM;EQ 15MG BASE
Approval Date
2009-05-12
Regulatory Status
Discontinued
Drug Name
ACTOPLUS MET XR
Product Number
2
Dosage Form
-
Strength
1GM;EQ 30MG BASE
Approval Date
2009-05-12
Active Ingredient
METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Application Number
22024
Product Number
2
Dosage Form
-
Strength
1GM;EQ 30MG BASE
Approval Date
2009-05-12
Regulatory Status
Discontinued
Drug Name
AGRYLIN
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-03-14
Active Ingredient
ANAGRELIDE HYDROCHLORIDE
Application Number
20333
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-03-14
Regulatory Status
Discontinued
Drug Name
CERADON
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1988-12-30
Active Ingredient
CEFOTIAM HYDROCHLORIDE
Application Number
50601
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1988-12-30
Regulatory Status
Discontinued
Drug Name
COLCRYS
Product Number
1
Dosage Form
-
Strength
0.6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-07-29
Active Ingredient
COLCHICINE
Application Number
22352
Product Number
1
Dosage Form
-
Strength
0.6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2009-07-29
Regulatory Status
Discontinued
Drug Name
DEXILANT SOLUTAB
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2016-01-26
Active Ingredient
DEXLANSOPRAZOLE
Application Number
208056
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2016-01-26
Regulatory Status
Discontinued
Drug Name
EXKIVITY
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE
Approval Date
2021-09-15
Active Ingredient
MOBOCERTINIB SUCCINATE
Application Number
215310
Product Number
1
Dosage Form
-
Strength
EQ 40MG BASE
Approval Date
2021-09-15
Regulatory Status
Discontinued
Drug Name
FOSRENOL
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2004-10-26
Active Ingredient
LANTHANUM CARBONATE
Application Number
21468
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE
Approval Date
2004-10-26
Regulatory Status
Discontinued
Drug Name
OMONTYS
Product Number
7
Dosage Form
-
Strength
EQ 10MG BASE/ML (EQ 10MG BASE/ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
7
Dosage Form
-
Strength
EQ 10MG BASE/ML (EQ 10MG BASE/ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OMONTYS
Product Number
8
Dosage Form
-
Strength
EQ 20MG BASE/2ML (EQ 10MG BASE/ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
8
Dosage Form
-
Strength
EQ 20MG BASE/2ML (EQ 10MG BASE/ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OMONTYS PRESERVATIVE FREE
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/0.5ML (EQ 1MG BASE/0.5ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/0.5ML (EQ 1MG BASE/0.5ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OMONTYS PRESERVATIVE FREE
Product Number
2
Dosage Form
-
Strength
EQ 2MG BASE/0.5ML (EQ 2MG BASE/0.5ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
2
Dosage Form
-
Strength
EQ 2MG BASE/0.5ML (EQ 2MG BASE/0.5ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OMONTYS PRESERVATIVE FREE
Product Number
3
Dosage Form
-
Strength
EQ 3MG BASE/0.5ML (EQ 3MG BASE/0.5ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
3
Dosage Form
-
Strength
EQ 3MG BASE/0.5ML (EQ 3MG BASE/0.5ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OMONTYS PRESERVATIVE FREE
Product Number
4
Dosage Form
-
Strength
EQ 4MG BASE/0.5ML (EQ 4MG BASE/0.5ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
4
Dosage Form
-
Strength
EQ 4MG BASE/0.5ML (EQ 4MG BASE/0.5ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OMONTYS PRESERVATIVE FREE
Product Number
5
Dosage Form
-
Strength
EQ 5MG BASE/0.5ML (EQ 5MG BASE/0.5ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
5
Dosage Form
-
Strength
EQ 5MG BASE/0.5ML (EQ 5MG BASE/0.5ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OMONTYS PRESERVATIVE FREE
Product Number
6
Dosage Form
-
Strength
EQ 6MG BASE/0.5ML (EQ 6MG BASE/0.5ML)
Approval Date
2012-03-27
Active Ingredient
PEGINESATIDE ACETATE
Application Number
202799
Product Number
6
Dosage Form
-
Strength
EQ 6MG BASE/0.5ML (EQ 6MG BASE/0.5ML)
Approval Date
2012-03-27
Regulatory Status
Discontinued
Drug Name
OSENI
Product Number
4
Dosage Form
-
Strength
EQ 12.5MG BASE;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2013-01-25
Active Ingredient
ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
Application Number
22426
Product Number
4
Dosage Form
-
Strength
EQ 12.5MG BASE;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2013-01-25
Regulatory Status
Discontinued
Drug Name
OSENI
Product Number
6
Dosage Form
-
Strength
EQ 12.5MG BASE;EQ 45MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2013-01-25
Active Ingredient
ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
Application Number
22426
Product Number
6
Dosage Form
-
Strength
EQ 12.5MG BASE;EQ 45MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2013-01-25
Regulatory Status
Discontinued
Drug Name
PREVACID
Product Number
1
Dosage Form
-
Strength
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-05-10
Active Ingredient
LANSOPRAZOLE
Application Number
20406
Product Number
1
Dosage Form
-
Strength
15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-05-10
Regulatory Status
Discontinued
Drug Name
PREVACID
Product Number
1
Dosage Form
-
Strength
15MG/PACKET
Approval Date
2001-05-03
Active Ingredient
LANSOPRAZOLE
Application Number
21281
Product Number
1
Dosage Form
-
Strength
15MG/PACKET
Approval Date
2001-05-03
Regulatory Status
Discontinued
Drug Name
PREVACID
Product Number
2
Dosage Form
-
Strength
30MG/PACKET
Approval Date
2001-05-03
Active Ingredient
LANSOPRAZOLE
Application Number
21281
Product Number
2
Dosage Form
-
Strength
30MG/PACKET
Approval Date
2001-05-03
Regulatory Status
Discontinued
Drug Name
PREVACID IV
Product Number
1
Dosage Form
-
Strength
30MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2004-05-27
Active Ingredient
LANSOPRAZOLE
Application Number
21566
Product Number
1
Dosage Form
-
Strength
30MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2004-05-27
Regulatory Status
Discontinued
Drug Name
PREVACID NAPRAPAC 250 (COPACKAGED)
Product Number
2
Dosage Form
-
Strength
15MG,N/A;N/A,250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-11-14
Active Ingredient
LANSOPRAZOLE; NAPROXEN
Application Number
21507
Product Number
2
Dosage Form
-
Strength
15MG,N/A;N/A,250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2003-11-14
Regulatory Status
Discontinued
Drug Name
PREVACID NAPRAPAC 375 (COPACKAGED)
Product Number
3
Dosage Form
-
Strength
15MG,N/A;N/A,375MG
Approval Date
2003-11-14
Active Ingredient
LANSOPRAZOLE; NAPROXEN
Application Number
21507
Product Number
3
Dosage Form
-
Strength
15MG,N/A;N/A,375MG
Approval Date
2003-11-14
Regulatory Status
Discontinued
Drug Name
PREVACID NAPRAPAC 500 (COPACKAGED)
Product Number
4
Dosage Form
-
Strength
15MG,N/A;N/A,500MG
Approval Date
2003-11-14
Active Ingredient
LANSOPRAZOLE; NAPROXEN
Application Number
21507
Product Number
4
Dosage Form
-
Strength
15MG,N/A;N/A,500MG
Approval Date
2003-11-14
Regulatory Status
Discontinued
Drug Name
PREVPAC (COPACKAGED)
Product Number
1
Dosage Form
-
Strength
500MG;500MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-12-02
Active Ingredient
AMOXICILLIN; CLARITHROMYCIN; LANSOPRAZOLE
Application Number
50757
Product Number
1
Dosage Form
-
Strength
500MG;500MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1997-12-02
Regulatory Status
Discontinued
Drug Name
PROAMATINE
Product Number
1
Dosage Form
-
Strength
2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-09-06
Active Ingredient
MIDODRINE HYDROCHLORIDE
Application Number
19815
Product Number
1
Dosage Form
-
Strength
2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-09-06
Regulatory Status
Discontinued
Drug Name
PROAMATINE
Product Number
2
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-09-06
Active Ingredient
MIDODRINE HYDROCHLORIDE
Application Number
19815
Product Number
2
Dosage Form
-
Strength
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-09-06
Regulatory Status
Discontinued
Drug Name
PROAMATINE
Product Number
3
Dosage Form
-
Strength
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2002-03-20
Active Ingredient
MIDODRINE HYDROCHLORIDE
Application Number
19815
Product Number
3
Dosage Form
-
Strength
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2002-03-20
Regulatory Status
Discontinued
Drug Name
TRINTELLIX
Product Number
3
Dosage Form
-
Strength
EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2013-09-30
Active Ingredient
VORTIOXETINE HYDROBROMIDE
Application Number
204447
Product Number
3
Dosage Form
-
Strength
EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2013-09-30
Regulatory Status
Discontinued
Drug Status Breakdown
31 total- Discontinued
Official Source
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Drug Name
ACTOPLUS MET
Application Number
21842
Product Number
1
Active Ingredient
METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
Dosage Form
-
Strength
500MG;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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