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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 019465
Company: HOSPIRA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 900MG/100ML SOLUTION;INJECTION Prescription AP Yes Yes
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 450MG/50ML (9MG/ML) SOLUTION;INJECTION Prescription AP Yes No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
07/15/1985 ORIG-1 Approval Type 5 - New Formulation or New Manufacturer STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/29/2019 SUPPL-58 Labeling-Package Insert

Label is not available on this site.

09/27/2016 SUPPL-55 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019465s055lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/019465Orig1s055ltr.pdf
06/10/2016 SUPPL-54 Labeling-Container/Carton Labels Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/019465Orig1s054,019466Orig1s057,019479Orig1s049,019480Orig1s045,019759Orig1s046ltr.pdf
11/01/2002 SUPPL-38 Manufacturing (CMC)-Packaging

Label is not available on this site.

04/06/2000 SUPPL-37 Manufacturing (CMC)-Expiration Date

Label is not available on this site.

04/06/2000 SUPPL-36 Labeling

Label is not available on this site.

04/06/2000 SUPPL-35 Manufacturing (CMC)-Packaging

Label is not available on this site.

12/01/1998 SUPPL-34 Manufacturing (CMC)

Label is not available on this site.

08/20/1997 SUPPL-33 Manufacturing (CMC)

Label is not available on this site.

06/11/1997 SUPPL-32 Manufacturing (CMC)

Label is not available on this site.

07/02/1999 SUPPL-31 Labeling

Label is not available on this site.

03/04/1996 SUPPL-30 Manufacturing (CMC)

Label is not available on this site.

05/31/1995 SUPPL-29 Manufacturing (CMC)

Label is not available on this site.

08/27/1996 SUPPL-28 Manufacturing (CMC)

Label is not available on this site.

01/24/1996 SUPPL-27 Manufacturing (CMC)

Label is not available on this site.

09/23/1994 SUPPL-26 Manufacturing (CMC)

Label is not available on this site.

01/05/1995 SUPPL-25 Manufacturing (CMC)

Label is not available on this site.

06/21/1994 SUPPL-24 Labeling

Label is not available on this site.

02/25/1994 SUPPL-23 Manufacturing (CMC)

Label is not available on this site.

12/30/1991 SUPPL-20 Manufacturing (CMC)

Label is not available on this site.

01/28/1992 SUPPL-17 Manufacturing (CMC)

Label is not available on this site.

09/10/1991 SUPPL-16 Manufacturing (CMC)

Label is not available on this site.

02/16/1993 SUPPL-15 Labeling

Label is not available on this site.

11/02/1990 SUPPL-14 Manufacturing (CMC)

Label is not available on this site.

01/11/1990 SUPPL-13 Manufacturing (CMC)

Label is not available on this site.

03/09/1990 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

02/22/1990 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

08/03/1989 SUPPL-10 Manufacturing (CMC)

Label is not available on this site.

07/18/1989 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

09/20/1989 SUPPL-8 Labeling

Label is not available on this site.

02/06/1989 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

11/26/1986 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

08/08/1986 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

05/27/1986 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

01/17/1986 SUPPL-1 Labeling

Label is not available on this site.

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
09/27/2016 SUPPL-55 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019465s055lbl.pdf

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

SOLUTION;INJECTION; 900MG/100ML
TE Code = AP

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 900MG/100ML SOLUTION;INJECTION Prescription Yes AP 016677 BAXTER HLTHCARE
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 900MG/100ML SOLUTION;INJECTION Prescription Yes AP 020178 BAXTER HLTHCARE
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 900MG/100ML SOLUTION;INJECTION Prescription Yes AP 019465 HOSPIRA
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 900MG/100ML SOLUTION;INJECTION Prescription No AP 211968 NEPHRON

SOLUTION;INJECTION; 450MG/50ML (9MG/ML)
TE Code = AP

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 450MG/50ML (9MG/ML) SOLUTION;INJECTION Prescription Yes AP 016677 BAXTER HLTHCARE
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 450MG/50ML (9MG/ML) SOLUTION;INJECTION Prescription Yes AP 020178 BAXTER HLTHCARE
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 450MG/50ML (9MG/ML) SOLUTION;INJECTION Prescription Yes AP 018803 HOSPIRA
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 450MG/50ML (9MG/ML) SOLUTION;INJECTION Prescription Yes AP 019465 HOSPIRA
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE 450MG/50ML (9MG/ML) SOLUTION;INJECTION Prescription No AP 211968 NEPHRON
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