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Bupropion Hydrochloride
Bupropion Hydrochloride - 68084-251-01 - (Bupropion Hydrochloride)
Drug Information of Bupropion Hydrochloride
| Product NDC: | 68084-251 |
| Proprietary Name: | Bupropion Hydrochloride |
| Non Proprietary Name: | Bupropion Hydrochloride |
| Active Ingredient(s): | 150 mg/1 & nbsp; Bupropion Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bupropion Hydrochloride
| Product NDC: | 68084-251 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077285 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130708 |
Package Information of Bupropion Hydrochloride
| Package NDC: | 68084-251-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-251-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-251-11) |
NDC Information of Bupropion Hydrochloride
| NDC Code | 68084-251-01 |
| Proprietary Name | Bupropion Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-251-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-251-11) |
| Product NDC | 68084-251 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bupropion Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130708 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | BUPROPION HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
