DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
POTASSIUM CHLORIDE
FDA Application No:
(ANDA) 080205
Active Ingredient(s):
POTASSIUM CHLORIDE
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
March 16, 1972
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
POTASSIUM CHLORIDE
POTASSIUM CHLORIDE
2MEQ/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
POTASSIUM CHLORIDE
POTASSIUM CHLORIDE
1MEQ/ML
INJECTABLE; INJECTION
Discontinued
No
None
POTASSIUM CHLORIDE
POTASSIUM CHLORIDE
2.4MEQ/ML
INJECTABLE; INJECTION
Discontinued
No
None
POTASSIUM CHLORIDE
POTASSIUM CHLORIDE
3.2MEQ/ML
INJECTABLE; INJECTION
Discontinued
No
None
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