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NDC 43547-0290-50 bupropion 200 mg/1 Details
bupropion 200 mg/1
bupropion is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Solco Healthcare US LLC. The primary component is BUPROPION HYDROCHLORIDE.
MedlinePlus Drug Summary
Bupropion (Aplenzin, Wellbutrin, Wellbutrin SR, Wellbutrin XL) is used to treat depression. Bupropion (Aplenzin, Wellbutrin XL) is also used to treat seasonal affective disorder (SAD; episodes of depression that occur at the same time each year [usually in the fall and winter but rarely may occur in the spring or summer months]). Bupropion (Zyban) is used to help people stop smoking. Bupropion is in a class of medications called antidepressants. It works by increasing certain types of activity in the brain.
Related Packages: 43547-0290-50Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Bupropion
Product Information
| NDC | 43547-0290 |
|---|---|
| Product ID | 43547-290_8978516f-6290-434f-9166-ff3007f0881f |
| Associated GPIs | 58300040107440 |
| GCN Sequence Number | 050496 |
| GCN Sequence Number Description | bupropion HCl TAB SR 12H 200 MG ORAL |
| HIC3 | H7D |
| HIC3 Description | NOREPINEPHRINE AND DOPAMINE REUPTAKE INHIB (NDRIS) |
| GCN | 17573 |
| HICL Sequence Number | 001653 |
| HICL Sequence Number Description | BUPROPION HCL |
| Brand/Generic | Generic |
| Proprietary Name | bupropion |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | bupropion hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 200 |
| Active Ingredient Units | mg/1 |
| Substance Name | BUPROPION HYDROCHLORIDE |
| Labeler Name | Solco Healthcare US LLC |
| Pharmaceutical Class | Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA202304 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43547-0290-50 (43547029050)
| NDC Package Code | 43547-290-50 |
|---|---|
| Billing NDC | 43547029050 |
| Package | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-290-50) |
| Marketing Start Date | 2014-11-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |