Bupropion Hydrochloride
- Product NDC
- 71205-387
- 11-digit product format
- 712050387
- Labeler code
- 71205
- Product ID
- 71205-387_079d1cc7-db71-4327-b73d-e094b345ae05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075932
- Marketing category
- ANDA
- Marketing start
- 2003-11-25
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-387 | BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE [PROFICIENT RX LP] | 1 | Legacy NDC | 20200121_079d1cc7-db71-4327-b73d-e094b345ae05.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-387-30 | 71205038730 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-387-30) | 2020-01-15 | 0000-00-00 | No | No | Current |
| 71205-387-60 | 71205038760 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-387-60) | 2020-01-15 | 0000-00-00 | No | No | Current |
| 71205-387-90 | 71205038790 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-387-90) | 2020-01-15 | 0000-00-00 | No | No | Current |