Bupropion Hydrochloride
- Product NDC
- 55289-733
- 11-digit product format
- 552890733
- Labeler code
- 55289
- Product ID
- 55289-733_a6bba2cd-8071-092c-e053-2a95a90a2231
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075491
- Marketing category
- ANDA
- Marketing start
- 2000-05-11
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 100 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-733-30 | 55289073330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-733-30) | 2010-01-25 | 0000-00-00 | No | No | Current |
| 55289-733-60 | 55289073360 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-733-60) | 2010-01-25 | 0000-00-00 | No | No | Current |