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 |