NDC 69097-875 – Bupropion Hydrochloride (XL)
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC69097-875
Product details
- Brand name
- Bupropion Hydrochloride (XL)
- Generic name
- Bupropion hydrochloride
- Labeler
- CIPLA USA INC.,
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA206556
- Marketed since
- August 29, 2016
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 69097-875-02 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-02) | Aug 29, 2016 |
| 69097-875-05 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-05) | Aug 29, 2016 |
| 69097-875-12 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-12) | Aug 29, 2016 |
Recalls mentioning this NDC
- D-1212-2018 Sep 26, 2018 · Class III
Failed impurities/ degradation specifications: Out-of-specification results were observed in the meta-chlorobenzoic acid impurity in batches 18 months or older from date of manufacture in the 90…
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