HEPARIN SODIUM AND SODIUM CHLORIDE- heparin sodium injection, solution 
Baxter Healthcare Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Heparin Sodium bp 2000 iu/l in
0.9% w/v sodium chloride iv infusion

HEALTH CARE PROVIDER LETTER

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PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

Drug Shortage Heparin Representative Container Label 1

Container Label

Code B0953G
500 ml
Baxter Logo
Heparin Sodium BP 2000 IU/L in
0.9% w/v Sodium Chloride IV Infusion

VIAFLEX container

Sterile nonpyrogenic
Solution for Infusion
Single Dose

Each 500 ml contains
Heparin Sodium (Mucous) 1000 IU
Sodium Chloride 4.5 g
Disodium Phosphate 12H 2 0 2.9 g
Citric Acid (Monohydrate) 0.202g
Water for Injections

mmol per 500 ml (approx)
Sodium 93
Chloride 77
Phosphate 8
Citrate 1

For intravenous administration
Store out of reach and sight of children
Do not remove from overwrap until ready for use
Do not use unless solution is clear and container is
undamaged
Do not add any supplementary medication
For use under medical supervision
Do not store above 25°C
Discard any unused portion
Do not reconnect partially used bags
Baxter Healthcare Ltd
Thetford Norfolk IP24 3SE
PL00116/0130
POM symbol
Heparin Sodium BP 2000 IU/L in
0.9% w/v Sodium Chloride
IV Infusion

TH-35-01-749
Lot
Expiry
1
2
3
4

Drug Shortage Heparin Representative Container Label 2

Container Label

Code B0944
1000 ml
Baxter Logo
Heparin Sodium BP 2000 IU/L in
0.9% w/v Sodium Chloride IV Infusion

VIAFLEX container
Sterile nonpyrogenic
Solution for Infusion
Single Dose

 
Each 1000 ml contains
Heparin Sodium (Mucous) 2000 IU
Sodium Chloride 9 g
Disodium Phosphate 12H 2 0 5.8 g
Citric Acid (Monohydrate) 0.405 g
Water for Injections

mmol per 1000 ml (approx)
Sodium 186
Chloride 154
Phosphate 16
Citrate 2

For intravenous administration
Store out of reach and sight of children
Do not remove from overwrap until ready for
use
Do not use unless solution is clear and container
is undamaged
Do not add any supplementary medication
For use under medical supervision
Do not store above 25°C
Discard any unused portion
Do not reconnect partially used bags

Baxter Healthcare Ltd
Thetford Norfolk IP24 3SE
PL00116/0130
POM symbol
TH-35-01-237

Heparin Sodium BP 2000 IU/L in
0.9% w/v Sodium Chloride
IV Infusion

Lot
Expiry
1
2
3
4
5
6
7
8
9

HEPARIN SODIUM AND SODIUM CHLORIDE 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0338-9556
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HEPARIN SODIUM (UNII: ZZ45AB24CA) (HEPARIN - UNII:T2410KM04A) HEPARIN1000 [iU]  in 500 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 4.5 g  in 500 mL
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) 2.9 g  in 500 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 0.202 g  in 500 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0338-9556-2020 in 1 CARTON10/25/201708/31/2020
1500 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug for use in drug shortage10/25/201708/31/2020
HEPARIN SODIUM AND SODIUM CHLORIDE 
heparin sodium injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0338-9552
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HEPARIN SODIUM (UNII: ZZ45AB24CA) (HEPARIN - UNII:T2410KM04A) HEPARIN2000 [iU]  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 g  in 1000 mL
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) 5.8 g  in 1000 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 0.405 g  in 1000 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0338-9552-1010 in 1 CARTON10/25/201710/25/2017
11000 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug for use in drug shortage10/25/201710/25/2017
Labeler - Baxter Healthcare Corporation (005083209)
Establishment
NameAddressID/FEIBusiness Operations
Baxter Healthcare Ltd221478644ANALYSIS(0338-9556, 0338-9552) , MANUFACTURE(0338-9556, 0338-9552) , LABEL(0338-9556, 0338-9552) , PACK(0338-9556, 0338-9552) , STERILIZE(0338-9556, 0338-9552)

Revised: 7/2020
 
Baxter Healthcare Corporation