NDC 72189-134 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC72189-134
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- DIRECT RX
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- October 15, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72189-134-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-30) | Oct 15, 2020 |
| 72189-134-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-60) | Oct 15, 2020 |
| 72189-134-72 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-72) | Oct 15, 2020 |
| 72189-134-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-90) | Oct 15, 2020 |
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