Norpramin / desipramine hydrochloride FDA New drug application 014399 international drug patent coverage, generic alternatives and suppliers

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399	NDA	Validus Pharmaceuticals LLC	30698-007	30698-007-01	100 TABLET, SUGAR COATED in 1 BOTTLE (30698-007-01)
NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399	NDA	Validus Pharmaceuticals LLC	30698-011	30698-011-01	100 TABLET, SUGAR COATED in 1 BOTTLE (30698-011-01)

Tradename

Generic Name

Dosage

NDA

Application Type

Supplier

National Drug Code

Package Code

Package

TABLET;ORAL

NDA

30698-007

30698-007-01

100 TABLET, SUGAR COATED in 1 BOTTLE (30698-007-01)

TABLET;ORAL

NDA

30698-011

30698-011-01

100 TABLET, SUGAR COATED in 1 BOTTLE (30698-011-01)

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Validus Pharms	NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399-001	Approved Prior to Jan 1, 1982	⤷ Try a Trial	⤷ Try a Trial
Validus Pharms	NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399-001	Approved Prior to Jan 1, 1982	⤷ Try a Trial	⤷ Try a Trial
Validus Pharms	NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399-003	Approved Prior to Jan 1, 1982	⤷ Try a Trial	⤷ Try a Trial
Validus Pharms	NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399-007	Feb 11, 1982	⤷ Try a Trial	⤷ Try a Trial
Validus Pharms	NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399-006	Approved Prior to Jan 1, 1982	⤷ Try a Trial	⤷ Try a Trial
Validus Pharms	NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399-005	Approved Prior to Jan 1, 1982	⤷ Try a Trial	⤷ Try a Trial
Validus Pharms	NORPRAMIN	desipramine hydrochloride	TABLET;ORAL	014399-003	Approved Prior to Jan 1, 1982	⤷ Try a Trial	⤷ Try a Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	25MG
Approval Date:	Approved Prior to Jan 1, 1982	TE:	AB	RLD:	Yes

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	50MG
Approval Date:	Approved Prior to Jan 1, 1982	TE:	AB	RLD:	Yes

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	75MG
Approval Date:	Approved Prior to Jan 1, 1982	TE:	AB	RLD:	Yes

Details for New Drug Application (NDA): 014399