NDC 16571-402 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC16571-402
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077829
- Marketed since
- October 1, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cetirizine hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 16571-402-10 | 100 TABLET in 1 BOTTLE (16571-402-10) | Oct 1, 2009 |
| 16571-402-30 | 300 TABLET in 1 BOTTLE (16571-402-30) | May 10, 2026 |
| 16571-402-50 | 500 TABLET in 1 BOTTLE (16571-402-50) | Oct 1, 2009 |
Recalls mentioning this NDC
- D-0032-2026 Oct 29, 2025 · Class III
Tablet/Capsules Imprinted with Wrong ID - D-0033-2026 Oct 29, 2025 · Class III
Tablet/Capsules Imprinted with Wrong ID
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