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WELLBUTRIN XL
WELLBUTRIN XL - 21695-137-30 - (bupropion hydrochloride)
Drug Information of WELLBUTRIN XL
| Product NDC: | 21695-137 |
| Proprietary Name: | WELLBUTRIN XL |
| 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 WELLBUTRIN XL
| Product NDC: | 21695-137 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021515 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091223 |
Package Information of WELLBUTRIN XL
| Package NDC: | 21695-137-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-137-30) |
NDC Information of WELLBUTRIN XL
| NDC Code | 21695-137-30 |
| Proprietary Name | WELLBUTRIN XL |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-137-30) |
| Product NDC | 21695-137 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bupropion hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091223 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| 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] |
