Bupropion Hydrochloride
- Product NDC
- 60429-217
- 11-digit product format
- 604290217
- Labeler code
- 60429
- Product ID
- 60429-217_b7a0a352-f67c-6dd5-e053-2995a90a4be0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA079095
- Marketing category
- ANDA
- Marketing start
- 2009-03-24
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 60429-217-25 | 60429021725 | 250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60429-217-25) | 2014-06-24 | 0000-00-00 | No | No | Current |