BUDEPRION SR is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Bupropion Hydrochloride.
Product ID | 63629-2873_763ec70c-b853-4664-a648-74046636e1b2 |
NDC | 63629-2873 |
Product Type | Human Prescription Drug |
Proprietary Name | BUDEPRION SR |
Generic Name | Bupropion Hydrochloride |
Dosage Form | Tablet, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2004-03-23 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA075913 |
Labeler Name | Bryant Ranch Prepack |
Substance Name | BUPROPION HYDROCHLORIDE |
Active Ingredient Strength | 150 mg/1 |
Pharm Classes | Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2004-03-23 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA075913 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-03-23 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA075913 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-03-23 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA075913 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-03-23 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA075913 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-03-23 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA075913 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-06-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA075913 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-06-02 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
BUPROPION HYDROCHLORIDE | 150 mg/1 |
SPL SET ID: | c3ce7349-8ef2-4e66-a7d7-24fe71d18866 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
63629-2873 | BUDEPRION SR | BUDEPRION SR |
0115-5445 | Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE |
0115-6811 | Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE |
0185-0410 | Bupropion Hydrochloride | Bupropion Hydrochloride |
0185-0415 | Bupropion Hydrochloride | Bupropion Hydrochloride |
0185-1111 | Bupropion Hydrochloride | Bupropion Hydrochloride |
0173-0135 | WELLBUTRIN | bupropion hydrochloride |
0173-0722 | WELLBUTRIN | bupropion hydrochloride |
0173-0947 | WELLBUTRIN | bupropion hydrochloride |
0173-0556 | ZYBAN | bupropion hydrochloride |