Bupropion Hydrochloride
- Product NDC
- 55700-779
- 11-digit product format
- 557000779
- Labeler code
- 55700
- Product ID
- 55700-779_370d2e20-cda2-4ffc-bf22-bdd2af3ff8f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA076143
- Marketing category
- ANDA
- Marketing start
- 2019-07-26
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-779-30 | 55700077930 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-779-30) | 2021-09-10 | 0000-00-00 | No | No | Current |
| 55700-779-60 | 55700077960 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-779-60) | 2019-07-26 | 0000-00-00 | No | No | Current |