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BUPROPION HYDROCHLORIDE
BUPROPION HYDROCHLORIDE - 10370-101-09 - (bupropion hydrochloride)
Drug Information of BUPROPION HYDROCHLORIDE
| Product NDC: | 10370-101 |
| 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, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BUPROPION HYDROCHLORIDE
| Product NDC: | 10370-101 |
| Labeler Name: | Par Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077284 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081125 |
Package Information of BUPROPION HYDROCHLORIDE
| Package NDC: | 10370-101-09 |
| Package Description: | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-101-09) |
NDC Information of BUPROPION HYDROCHLORIDE
| NDC Code | 10370-101-09 |
| Proprietary Name | BUPROPION HYDROCHLORIDE |
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-101-09) |
| Product NDC | 10370-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bupropion hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20081125 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc. |
| 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] |
