Bupropion Hydrochloride
- Product NDC
- 68084-252
- 11-digit product format
- 680840252
- Labeler code
- 68084
- Product ID
- 68084-252_df3aeb24-dee2-e546-e053-2a95a90a9728
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077284
- Marketing category
- ANDA
- Marketing start
- 2008-06-05
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 300 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
- 2023-12-31
- 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 |
|---|
| 68084-252-21 | 68084025221 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-252-21) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-252-11) | 30 blister pack | 2008-06-05 | 0000-00-00 | No | No | Current |