DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CEFTAZIDIME
FDA Application No:
(ANDA) 062640
Active Ingredient(s):
CEFTAZIDIME
Company:
ACS DOBFAR
Original Approval or Tentative Approval Date:
November 20, 1985
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
CEFTAZIDIME
CEFTAZIDIME
500MG/VIAL
INJECTABLE; INJECTION
Prescription
No
AP
CEFTAZIDIME
CEFTAZIDIME
1GM/VIAL
INJECTABLE; INJECTION
Prescription
No
AP
CEFTAZIDIME
CEFTAZIDIME
2GM/VIAL
INJECTABLE; INJECTION
Prescription
No
AP
CEFTAZIDIME
CEFTAZIDIME
6GM/VIAL
INJECTABLE; INJECTION
Prescription
No
AP
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