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Approved Drug Products containing Terbutaline Sulfate listed in the FDA Orange Book. Original Data : FDA Website

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01 SANOFI AVENTIS US (4)

02 DR REDDYS (1)

03 ANI PHARMS (2)

04 AREVA PHARMS (1)

05 CHARTWELL INJECTABLE (1)

06 EPIC PHARMA LLC (1)

07 FRESENIUS KABI USA (1)

08 HIKMA FARMACEUTICA (1)

09 IMPAX LABS (2)

10 LANNETT CO INC (2)

11 NOVARTIS (1)

12 PHARMACARE (1)

13 TWI PHARMS (2)

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01 AEROSOL, METERED;INHALATION (2)

02 INJECTABLE;INJECTION (8)

03 TABLET;ORAL (10)

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01 DISCN (8)

02 RX (12)

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01 BRETHAIRE (1)

02 BRETHINE (3)

03 BRICANYL (4)

04 TERBUTALINE SULFATE (12)

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01 No (17)

02 Yes (3)

URL Supplier Web Content
INJECTABLE;INJECTION
1MG/ML
1982-01-01
17466
BRICANYL
DISCN
No
Sanofi Company Banner

IPS 2024

Not Confirmed

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URL Supplier Web Content
INJECTABLE;INJECTION
1MG/ML
2004-07-20
76853
TERBUTALINE SULFATE
DISCN
No
URL Supplier Web Content
TABLET;ORAL
2.5MG
1982-01-01
17618
BRICANYL
DISCN
No
Sanofi Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET;ORAL
5MG
1982-01-01
17618
BRICANYL
DISCN
No
Sanofi Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
AEROSOL, METERED;INHALATION
0.2MG/INH
1985-03-19
18000
BRICANYL
DISCN
No
Sanofi Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET;ORAL
2.5MG
1982-01-01
17849
BRETHINE
RX
Yes
AB
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URL Supplier Web Content
TABLET;ORAL
5MG
1982-01-01
17849
BRETHINE
RX
Yes
AB
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URL Supplier Web Content
TABLET;ORAL
2.5MG
2001-06-26
75877
TERBUTALINE SULFATE
RX
No
AB
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AEROSOL, METERED;INHALATION
0.2MG/INH
1984-08-17
18762
BRETHAIRE
DISCN
No
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INJECTABLE;INJECTION
1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
18571
BRETHINE
DISCN
Yes
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