NDC Code(s) : 70436-010-04, 70436-010-06, 70436-010-02, 70436-011-04, 70436-011-06, 70436-011-02
Packager : Slate Run Pharmaceuticals, LLC
Category : HUMAN PRESCRIPTION DRUG LABEL
DEA Schedule : none
Marketing Status : New Drug Application
INGREDIENTS AND APPEARANCE
Bupropion Hydrochloride bupropion hydrochloride TABLET, EXTENDED RELEASE | ||||||||||||||||||||||||||||||||||
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Bupropion Hydrochloride bupropion hydrochloride TABLET, EXTENDED RELEASE | ||||||||||||||||||||||||||||||||||
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LABELER - Slate Run Pharmaceuticals, LLC(039452765) |
REGISTRANT - Yichang Humanwell Pharmaceutical Co., Ltd.(527225336) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
Yichang Humanwell Oral Solid Dosage Plant | 421371958 | manufacture(70436-010, 70436-011) |
PRINCIPAL DISPLAY PANEL
NDC 70436-010-04
Rx only
ONCE-DAILY
Bupropion Hydrochloride Extended-release Tablets
150 mg
30 Tablets
WARNING: Do not use in combination with ZYBAN ® or any other medicines that contain bupropion hydrochloride.
PHARMACIST: Dispense the Medication Guide provided separately to each patient.
ZYBAN ® is registered trademark of GlaxoSmithKline.
NDC 70436-010-06
Rx only
ONCE-DAILY
Bupropion Hydrochloride Extended-release Tablets
150 mg
90 Tablets
WARNING: Do not use in combination with ZYBAN ® or any other medicines that contain bupropion hydrochloride.
PHARMACIST: Dispense the Medication Guide provided separately to each patient.
ZYBAN ® is registered trademark of GlaxoSmithKline.
NDC 70436-010-02
Rx only
ONCE-DAILY
Bupropion Hydrochloride Extended-release Tablets
150 mg
500 Tablets
WARNING: Do not use in combination with ZYBAN ® or any other medicines that contain bupropion hydrochloride.
PHARMACIST: Dispense the Medication Guide provided separately to each patient. .
ZYBAN ® is registered trademark of GlaxoSmithKline.
PRINCIPAL DISPLAY PANEL
NDC 70436-011-04
Rx only
ONCE-DAILY
Bupropion Hydrochloride Extended-release Tablets
300 mg
30 Tablets
WARNING: Do not use in combination with ZYBAN ® or any other medicines that contain bupropion hydrochloride.
PHARMACIST: Dispense the Medication Guide provided separately to each patient.
ZYBAN ® is registered trademark of GlaxoSmithKline.
NDC 70436-011-06
Rx only
ONCE-DAILY
Bupropion Hydrochloride Extended-release Tablets
300 mg
90 Tablets
WARNING: Do not use in combination with ZYBAN ® or any other medicines that contain bupropion hydrochloride.
PHARMACIST: Dispense the Medication Guide provided separately to each patient.
ZYBAN ® is registered trademark of GlaxoSmithKline.
NDC 70436-011-02
Rx only
ONCE-DAILY
Bupropion Hydrochloride Extended-release Tablets
300 mg
500 Tablets
WARNING: Do not use in combination with ZYBAN ® or any other medicines that contain bupropion hydrochloride.
PHARMACIST: Dispense the Medication Guide provided separately to each patient.
ZYBAN ® is registered trademark of GlaxoSmithKline.