NDC 65841-782 – buspirone hydrochloride
Buspirone Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC65841-782
Product details
- Brand name
- buspirone hydrochloride
- Generic name
- buspirone hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078888
- Marketed since
- May 3, 2014
- Listing expires
- December 31, 2027
Active ingredients
- Buspirone Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 65841-782-01 | 100 TABLET in 1 BOTTLE (65841-782-01) | May 3, 2014 |
| 65841-782-05 | 500 TABLET in 1 BOTTLE (65841-782-05) | May 3, 2014 |
| 65841-782-10 | 1000 TABLET in 1 BOTTLE (65841-782-10) | May 3, 2014 |
| 65841-782-77 | 100 BLISTER PACK in 1 CARTON (65841-782-77) / 1 TABLET in 1 BLISTER PACK (65841-782-30) | May 3, 2014 |
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