Bupropion Hydrochloride
- Product NDC
- 55154-4394
- 11-digit product format
- 551544394
- Labeler code
- 55154
- Product ID
- 55154-4394_8d44443e-89d9-40b5-a2e8-2a11af4a3ea9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075491
- Marketing category
- ANDA
- Marketing start
- 2000-07-01
- Marketing end
- 2021-02-28
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-4394-0 | 55154439400 | 10 BLISTER PACK in 1 BAG (55154-4394-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2000-07-01 | 2021-02-28 | No | No | Current |