Bupropion Hydrochloride
- Product NDC
- 43063-284
- 11-digit product format
- 430630284
- Labeler code
- 43063
- Product ID
- 43063-284_9db134ae-487f-15a7-e053-2a95a90a5c41
- 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
- 75 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 |
|---|
| 43063-284-30 | 43063028430 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-284-30) | 2010-01-25 | 0000-00-00 | No | No | Current |
| 43063-284-60 | 43063028460 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-284-60) | 2010-10-24 | 0000-00-00 | No | No | Current |
| 43063-284-98 | 43063028498 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-284-98) | 2010-10-24 | 0000-00-00 | No | No | Current |