NDC 68001-614 – Bupropion hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet · Oral
Product NDC68001-614
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA215568
- Marketed since
- April 9, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68001-614-03 | 500 TABLET in 1 BOTTLE (68001-614-03) | Apr 9, 2024 |
| 68001-614-04 | 30 TABLET in 1 BOTTLE (68001-614-04) | Jun 20, 2024 |
| 68001-614-05 | 90 TABLET in 1 BOTTLE (68001-614-05) | Jun 20, 2024 |
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