NDC Code(s) : 42571-241-01, 42571-242-01
Packager : Micro Labs Limited
Category : HUMAN PRESCRIPTION DRUG LABEL
DEA Schedule : none
Marketing Status : New Drug Application
INGREDIENTS AND APPEARANCE
BUPROPION HYDROCHLORIDEBupropion Hydrochloride TABLET, FILM COATED | ||||||||||||||||||||||
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BUPROPION HYDROCHLORIDEBupropion Hydrochloride TABLET, FILM COATED | ||||||||||||||||||||||
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LABELER - Micro Labs Limited(862174955) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
Micro Labs Limited | 915793658 | analysis(42571-241, 42571-242), label(42571-241, 42571-242), manufacture(42571-241, 42571-242), pack(42571-241, 42571-242) |
PRINCIPAL DISPLAY PANEL
NDC 42571-241-01
Three Times Daily (After Initial Titration)
Bupropion Hydrochloride Tablets, USP
75 mg
PHARMACIST: Dispense the enclosed Medication Guide to each patient.
WARNING: Do not use with other medicines that contain bupropion hydrochloride.
Federal Law requires dispensing of Bupropion Hydrochloride Tablets USP with the Medication Guide under this label.
Rx Only
100 Tablets
MICRO LABS LIMITED
NDC 42571-242-01
Three Times Daily (After Initial Titration)
Bupropion Hydrochloride Tablets, USP
100 mg
PHARMACIST: Dispense the enclosed Medication Guide to each patient.
WARNING: Do not use with other medicines that contain bupropion hydrochloride.
Federal Law requires dispensing of Bupropion Hydrochloride Tablets USP with the Medication Guide under this label.
Rx Only
100 Tablets
MICRO LABS LIMITED