DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DURABOLIN
FDA Application No:
(NDA) 011891
Active Ingredient(s):
NANDROLONE PHENPROPIONATE
Company:
ORGANON USA INC
Original Approval or Tentative Approval Date:
October 30, 1959
Chemical Type:
1 New molecular entity (NME)
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
DURABOLIN
NANDROLONE PHENPROPIONATE
25MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
DURABOLIN
NANDROLONE PHENPROPIONATE
50MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
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