Bupropion Hydrochloride
- Product NDC
- 0904-6585
- 11-digit product format
- 009046585
- Labeler code
- 0904
- Product ID
- 0904-6585_1e0ea26d-24ab-40c5-b9ec-1a816a8d0da1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA075932
- Marketing category
- ANDA
- Marketing start
- 2004-03-22
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6585-61 | 00904658561 | 100 BLISTER PACK in 1 CARTON (0904-6585-61) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 100 blister pack | 2004-03-22 | 0000-00-00 | No | No | Current |