Bupropion Hydrochloride
- Product NDC
- 64980-202
- 11-digit product format
- 649800202
- Labeler code
- 64980
- Product ID
- 64980-202_74120afa-f695-48b1-9eef-36d58d56b906
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- Application
- ANDA203013
- Marketing category
- ANDA
- Marketing start
- 2018-06-18
- 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
- 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 |
|---|
| 64980-202-01 | 64980020201 | 100 TABLET, FILM COATED in 1 BOTTLE (64980-202-01) | 2018-06-18 | 0000-00-00 | No | No | Current |
| 64980-202-05 | 64980020205 | 500 TABLET, FILM COATED in 1 BOTTLE (64980-202-05) | 2018-06-18 | 0000-00-00 | No | No | Current |