Bupropion Hydrochloride
- Product NDC
- 60687-312
- 11-digit product format
- 606870312
- Labeler code
- 60687
- Product ID
- 60687-312_d65b5d9f-1051-607d-e053-2a95a90a868a
- 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
- 2017-04-12
- 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
- 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 |
|---|
| 60687-312-01 | 60687031201 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-312-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-312-11) | 100 blister pack | 2017-04-12 | 0000-00-00 | No | No | Current |