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MagnacortDrug - Magnacort The trade name of the product as shown on the labeling.
Dosage -
OINTMENT; TOPICAL
Active Ingredient(s) -
Hydrocortamate Hydrochloride
Strength -
0.5%
Applicant -
PFIZER
New Drug Application (NDA) Number -
010554
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Pfizer Laboratories Div Pfizer Inc
Magnacort
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