DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
INDERAL LA
FDA Application No:
(NDA) 018553
Active Ingredient(s):
PROPRANOLOL HYDROCHLORIDE
Company:
WYETH PHARMS INC
Original Approval or Tentative Approval Date:
April 19, 1983
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
INDERAL LA
PROPRANOLOL HYDROCHLORIDE
160MG
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
Yes
AB
INDERAL LA
PROPRANOLOL HYDROCHLORIDE
80MG
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
AB
INDERAL LA
PROPRANOLOL HYDROCHLORIDE
120MG
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
AB
INDERAL LA
PROPRANOLOL HYDROCHLORIDE
60MG
CAPSULE, EXTENDED RELEASE; ORAL
Prescription
No
AB
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