bupropion
- Product NDC
- 55700-644
- 11-digit product format
- 557000644
- Labeler code
- 55700
- Product ID
- 55700-644_f1fd4649-2377-4a7a-bfd4-e0afe18ae503
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202304
- Marketing category
- ANDA
- Marketing start
- 2018-06-22
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-644-30 | 55700064430 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-644-30) | 2018-06-22 | 0000-00-00 | No | No | Current |