DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TETRACYCLINE HYDROCHLORIDE
FDA Application No:
(ANDA) 060736
Active Ingredient(s):
TETRACYCLINE HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for TETRACYCLINE HYDROCHLORIDE, (ANDA) 060736
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/24/2002
023
Control Supplement
2/8/2002
022
Facility Addition
9/24/2001
021
Packager Addition
11/2/2001
020
Facility Addition
12/18/2000
019
Facility Addition
12/18/2000
018
Facility Addition
12/18/2000
017
Facility Addition
12/18/2000
016
Facility Addition
5/1/1992
015
Labeling
1/22/1992
014
Labeling
2/7/1980
000
Approval
Therapeutic Equivalents
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