Approved Drug Products containing Betamethasone Dipropionate listed in the FDA Orange Book. Original Data : FDA Website

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Not Confirmed

U.S.A

RLD : No

TE Code :

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 1987-06-17

Application Number : 71143

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

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Not Confirmed

U.S.A

RLD : No

TE Code :

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : LOTION;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 1988-08-24

Application Number : 72276

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

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Not Confirmed

U.S.A

RLD : No

TE Code : AB

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 1992-04-30

Application Number : 73552

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

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Not Confirmed

U.S.A

RLD : No

TE Code : AB

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 1994-09-15

Application Number : 74271

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

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Not Confirmed

U.S.A

RLD : No

TE Code :

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : LOTION;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 1994-09-30

Application Number : 74272

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

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Not Confirmed

U.S.A

RLD : No

TE Code : AB

BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE

Brand Name : CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 0.05% BASE;1%

Approval Date : 2001-05-29

Application Number : 75673

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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07

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Not Confirmed

U.S.A

RLD : No

TE Code : AB

BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE

Brand Name : CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE

Dosage Form : LOTION;TOPICAL

Dosage Strength : EQ 0.05% BASE;1%

Approval Date : 2004-07-28

Application Number : 76493

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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Not Confirmed

U.S.A

RLD : No

TE Code : AB

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : GEL, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 2003-12-02

Application Number : 76508

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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09

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Not Confirmed

U.S.A

RLD : No

TE Code : AB

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : CREAM, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 2003-12-09

Application Number : 76543

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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Not Confirmed

U.S.A

RLD : No

TE Code : AB

Brand Name : BETAMETHASONE DIPROPIONATE

Dosage Form : OINTMENT, AUGMENTED;TOPICAL

Dosage Strength : EQ 0.05% BASE

Approval Date : 2004-10-12

Application Number : 76753

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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