NDC 68084-697 – BuPROPion Hydrochloride
Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68084-697
Product details
- Brand name
- BuPROPion Hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079095
- Marketed since
- April 2, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68084-697-01 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-697-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-697-11) | Apr 2, 2015 |
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