NDC 16571-661 – Meclizine Hydrochloride
Meclizine Hydrochloride 25 mg/1 · Tablet · Oral
Product NDC16571-661
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA010721
- Marketed since
- January 15, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antiemetic
Active ingredients
- Meclizine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Meclizine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16571-661-01 | 100 TABLET in 1 BOTTLE (16571-661-01) | Jan 15, 2020 |
| 16571-661-10 | 1000 TABLET in 1 BOTTLE (16571-661-10) | Jan 15, 2020 |
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