NDC 63187-521 – bupropion
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC63187-521
Product details
- Brand name
- bupropion
- Generic name
- bupropion
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA201567
- Marketed since
- February 15, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63187-521-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-30) | Dec 1, 2018 |
| 63187-521-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-60) | Dec 1, 2018 |
| 63187-521-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-521-90) | Dec 1, 2018 |
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