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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 089070
Company: HOSPIRA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PROCAINAMIDE HYDROCHLORIDE PROCAINAMIDE HYDROCHLORIDE 500MG/ML INJECTABLE;INJECTION Prescription AP No Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
02/12/1986 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/05/1999 SUPPL-12 Labeling

Label is not available on this site.

02/12/1998 SUPPL-11 Labeling

Label is not available on this site.

05/05/1998 SUPPL-10 Manufacturing (CMC)-Microbiology-Processing

Label is not available on this site.

12/21/1998 SUPPL-9 Labeling

Label is not available on this site.

08/24/1994 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

12/22/1993 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

11/22/1991 SUPPL-5 Labeling

Label is not available on this site.

08/16/1990 SUPPL-4 Labeling

Label is not available on this site.

08/12/1988 SUPPL-3 Labeling

Label is not available on this site.

11/23/1988 SUPPL-2 Labeling

Label is not available on this site.

PROCAINAMIDE HYDROCHLORIDE

INJECTABLE;INJECTION; 500MG/ML
TE Code = AP

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
PROCAINAMIDE HYDROCHLORIDE PROCAINAMIDE HYDROCHLORIDE 500MG/ML INJECTABLE;INJECTION Prescription No AP 089070 HOSPIRA
PROCAINAMIDE HYDROCHLORIDE PROCAINAMIDE HYDROCHLORIDE 500MG/ML INJECTABLE;INJECTION Prescription No AP 206332 NEXUS
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