Orange Book product · Generic (ANDA)
PROCAINAMIDE HYDROCHLORIDE
PROCAINAMIDE HYDROCHLORIDE
At a glance
Nov 20, 1985
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 20, 1985
41 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
PROCAINAMIDE HYDROCHLORIDE
Strength
100MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 088824
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of PROCAINAMIDE HYDROCHLORIDE
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ANDA 206332 · NEXUS
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ANDA 040111 · ANI PHARMS
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ANDA 089528 · WARNER CHILCOTT
- 1988PROCAINAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 089529 · WARNER CHILCOTT
- 1987PROCAINAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 089537 · HOSPIRA
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ANDA 089415 · ABRAXIS PHARM
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ANDA 089416 · ABRAXIS PHARM
- 1986PROCAINAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 089219 · ANI PHARMS
- 1986PROCAINAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 089029 · HIKMA
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.
