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Approved Drug Products containing 1-naphthalen-1-yloxy-3-(propan-2-ylamino)propan-2-ol hydrochloride listed in the FDA Orange Book. Original Data : FDA Website

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01 6ACTAVIS ELIZABETH

02 4ADARE PHARMS INC

03 1AIPING PHARM INC

04 4AMTA

05 12ANI PHARMS

06 1BAXTER HLTHCARE CORP

07 1CHARTWELL INJECTABLE

08 7CHARTWELL RX

09 6DAVA PHARMS INC

10 8DURAMED PHARMS BARR

11 5ENDO OPERATIONS

12 4EXTROVIS

13 1FOSUN PHARMA

14 1FRESENIUS KABI USA

15 2HIKMA

16 1HIKMA FARMACEUTICA

17 5IMPAX LABS INC

18 5INNOGENIX

19 4INTERPHARM

20 4INWOOD LABS

21 5IPCA LABS LTD

22 7IVAX SUB TEVA PHARMS

23 4LEDERLE

24 4LUPIN LTD

25 6MYLAN

26 4NORTEC DEV ASSOC

27 5NORTHSTAR HLTHCARE

28 2PAI HOLDINGS PHARM

29 1PIERRE FABRE

30 5PUREPAC PHARM

31 2RISING

32 7ROXANE

33 6SANDOZ

34 5SCHERING

35 2SMITH AND NEPHEW

36 1SOLOPAK

37 4SUPERPHARM

38 3TEVA

39 4UPSHER SMITH LABS

40 1VINTAGE PHARMS

41 7WARNER CHILCOTT

42 23WATSON LABS

43 3WATSON LABS TEVA

44 4WYETH AYERST

45 6WYETH PHARMS

46 2WYETH PHARMS INC

47 4ZYDUS PHARMS USA INC

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PharmaCompass

01

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERAL LA

Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

Dosage Strength : 160MG

Approval Date : 1983-04-19

Application Number : 18553

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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02

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : PROPRANOLOL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 16419

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERAL

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 16418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERAL

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 16418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERAL

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 16418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERAL

Dosage Form : TABLET;ORAL

Dosage Strength : 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 16418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERAL

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-10-18

Application Number : 16418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERAL

Dosage Form : TABLET;ORAL

Dosage Strength : 90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-10-18

Application Number : 16418

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERIDE-40/25

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 18031

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

26th North American ISSX
Not Confirmed
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26th North American ISSX
Not Confirmed

HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE

Brand Name : INDERIDE-80/25

Dosage Form : TABLET;ORAL

Dosage Strength : 25MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 18031

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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