Bupropion Hydrochloride
- Product NDC
- 71335-0468
- 11-digit product format
- 713350468
- Labeler code
- 71335
- Product ID
- 71335-0468_44e8152a-7f02-41e0-b0d4-732339d36b82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075584
- Marketing category
- ANDA
- Marketing start
- 2000-02-07
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 71335-0468-1 | 71335046801 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0468-1) | 2007-03-08 | 0000-00-00 | No | No | Current |
| 71335-0468-2 | 71335046802 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0468-2) | 2007-03-08 | 0000-00-00 | No | No | Current |
| 71335-0468-3 | 71335046803 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0468-3) | 2007-03-08 | 0000-00-00 | No | No | Current |
| 71335-0468-4 | 71335046804 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0468-4) | 2007-03-08 | 0000-00-00 | No | No | Current |
| 71335-0468-5 | 71335046805 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0468-5) | 2007-03-08 | 0000-00-00 | No | No | Current |
| 71335-0468-6 | 71335046806 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0468-6) | 2007-03-08 | 0000-00-00 | No | No | Current |
| 71335-0468-7 | 71335046807 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0468-7) | 2007-03-08 | 0000-00-00 | No | No | Current |