DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FREAMINE 8.5%
FDA Application No:
(NDA) 016822
Active Ingredient(s):
AMINO ACIDS
Company:
B BRAUN
Original Approval or Tentative Approval Date:
September 24, 1971
Chemical Type:
4 New combination
Review Classification:
P Priority review drug
Therapeutic Equivalents
Label Information
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
FREAMINE 8.5%
AMINO ACIDS
8.5% (8.5GM/100ML)
INJECTABLE; INJECTION
Discontinued
No
None
FREAMINE HBC 6.9%
AMINO ACIDS
6.9% (6.9GM/100ML)
INJECTABLE; INJECTION
Prescription
No
None
FREAMINE II 8.5%
AMINO ACIDS
8.5% (8.5GM/100ML)
INJECTABLE; INJECTION
Discontinued
No
None
FREAMINE III 10%
AMINO ACIDS
10% (10GM/100ML)
INJECTABLE; INJECTION
Prescription
No
None
FREAMINE III 3% W/ ELECTROLYTES
AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
3%; 54MG/100ML; 40MG/100ML; 150MG/100ML; 200MG/100ML; 120MG/100ML
INJECTABLE; INJECTION
Prescription
No
None
FREAMINE III 8.5%
AMINO ACIDS
8.5% (8.5GM/100ML)
INJECTABLE; INJECTION
Prescription
No
None
FREAMINE III 8.5% W/ ELECTROLYTES
AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE
8.5%; 110MG/100ML; 230MG/100ML; 10MG/100ML; 440MG/100ML; 690MG/100ML
INJECTABLE; INJECTION
Prescription
No
None
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