DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HEPARIN LOCK FLUSH IN PLASTIC CONTAINER
FDA Application No:
(NDA) 005264
Active Ingredient(s):
HEPARIN SODIUM
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
May 4, 1943
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
HEPARIN LOCK FLUSH
HEPARIN SODIUM
10 UNITS/ML
INJECTABLE; INJECTION
Prescription
No
AP
HEPARIN LOCK FLUSH
HEPARIN SODIUM
100 UNITS/ML
INJECTABLE; INJECTION
Discontinued
No
None
HEPARIN LOCK FLUSH IN PLASTIC CONTAINER
HEPARIN SODIUM
10 UNITS/ML
INJECTABLE; INJECTION
Prescription
No
AP
HEPARIN LOCK FLUSH IN PLASTIC CONTAINER
HEPARIN SODIUM
100 UNITS/ML
INJECTABLE; INJECTION
Prescription
No
AP
HEPARIN SODIUM PRESERVATIVE FREE
HEPARIN SODIUM
2,000 UNITS/ML
INJECTABLE; INJECTION
Prescription
Yes
None
HEPARIN SODIUM PRESERVATIVE FREE
HEPARIN SODIUM
2,500 UNITS/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
PANHEPRIN
HEPARIN SODIUM
1,000 UNITS/ML
INJECTABLE; INJECTION
Discontinued
No
None
PANHEPRIN
HEPARIN SODIUM
5,000 UNITS/ML
INJECTABLE; INJECTION
Discontinued
No
None
PANHEPRIN
HEPARIN SODIUM
10,000 UNITS/ML
INJECTABLE; INJECTION
Discontinued
No
None
PANHEPRIN
HEPARIN SODIUM
20,000 UNITS/ML
INJECTABLE; INJECTION
Discontinued
No
None
PANHEPRIN
HEPARIN SODIUM
40,000 UNITS/ML
INJECTABLE; INJECTION
Discontinued
No
None
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