Orange Book product · Generic (ANDA)
CITALOPRAM HYDROBROMIDE
CITALOPRAM HYDROBROMIDE
At a glance
Mar 27, 2007
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 27, 2007
19 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
CITALOPRAM HYDROBROMIDE
Strength
EQ 10MG BASE
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 078216
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CITALOPRAM HYDROBROMIDE
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NDA 021763 · BIOVAIL LABS INTL
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NDA 020822 · ABBVIE
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NDA 021046 · FOREST LABS
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ANDA 219985 · AUROBINDO PHARMA LTD
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ANDA 205407 · JUBILANT GENERICS
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ANDA 201450 · HETERO LABS LTD III
- 2009CITALOPRAM HYDROBROMIDEGeneric (ANDA)
ANDA 077654 · GLENMARK PHARMS LTD
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ANDA 077141 · NATCO PHARMA LTD
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ANDA 077668 · PHARMOBEDIENT
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ANDA 077289 · AMNEAL PHARMS NY
- 2006CITALOPRAM HYDROBROMIDEGeneric (ANDA)
ANDA 077534 · INVAGEN PHARMS
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
