Drugs@FDA: FDA-Approved Drugs
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 | INJECTABLE;INJECTION | Prescription | AP | Yes | 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 |
|---|---|---|---|---|---|---|---|
| 09/17/1985 | 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-49 | Labeling-Package Insert |
Label is not available on this site. |
||
| 09/27/2016 | SUPPL-46 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019480s046lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/019480Orig1s046ltr.pdf | |
| 06/10/2016 | SUPPL-45 | 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-33 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
||
| 12/01/1998 | SUPPL-32 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 08/20/1997 | SUPPL-31 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 06/11/1997 | SUPPL-30 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 07/02/1999 | SUPPL-29 | Labeling |
Label is not available on this site. |
||
| 03/04/1996 | SUPPL-28 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 05/31/1995 | SUPPL-27 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 08/27/1996 | SUPPL-26 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 01/24/1996 | SUPPL-25 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 09/23/1994 | SUPPL-24 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 01/05/1995 | SUPPL-23 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 02/25/1994 | SUPPL-22 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 12/30/1991 | SUPPL-19 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 01/28/1992 | SUPPL-16 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 09/10/1991 | SUPPL-15 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 11/02/1990 | SUPPL-14 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 03/09/1990 | SUPPL-13 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 01/11/1990 | 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. |
||
| 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-46 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019480s046lbl.pdf |
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
INJECTABLE;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 | INJECTABLE;INJECTION | Prescription | Yes | AP | 017464 | B BRAUN |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 900MG/100ML | INJECTABLE;INJECTION | Prescription | Yes | AP | 019635 | B BRAUN |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 900MG/100ML | INJECTABLE;INJECTION | Prescription | No | AP | 207310 | FRESENIUS KABI USA |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 900MG/100ML | INJECTABLE;INJECTION | Prescription | No | AP | 078177 | FRESENIUS MEDCL |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 900MG/100ML | INJECTABLE;INJECTION | Prescription | No | AP | 076316 | HAEMONETICS |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 900MG/100ML | INJECTABLE;INJECTION | Prescription | Yes | AP | 019480 | HOSPIRA |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 900MG/100ML | INJECTABLE;INJECTION | Prescription | Yes | AP | 016366 | ICU MEDICAL INC |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 900MG/100ML | INJECTABLE;INJECTION | Prescription | No | AP | 207956 | LABORATORIOS GRIFOLS |