NDC 68001-520 – Bupropion Hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC68001-520
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- December 13, 2021
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 68001-520-03 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-520-03) | Dec 13, 2021 |
| 68001-520-04 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-520-04) | Dec 13, 2021 |
| 68001-520-05 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-520-05) | Dec 13, 2021 |
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