NDC 70010-127 – Bupropion Hydrochloride
Bupropion Hydrochloride 200 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70010-127
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA218385
- Marketed since
- March 31, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70010-127-03 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-03) | Mar 31, 2025 |
| 70010-127-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-05) | Mar 31, 2025 |
| 70010-127-06 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-127-06) | Mar 31, 2025 |
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