NDC 71205-164 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71205-164
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077829
- Marketed since
- October 1, 2009
- Listing expires
- December 31, 2026
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71205-164-15 | 15 TABLET in 1 BOTTLE (71205-164-15) | Dec 1, 2018 |
| 71205-164-30 | 30 TABLET in 1 BOTTLE (71205-164-30) | Dec 1, 2018 |
| 71205-164-60 | 60 TABLET in 1 BOTTLE (71205-164-60) | Dec 1, 2018 |
| 71205-164-90 | 90 TABLET in 1 BOTTLE (71205-164-90) | Dec 1, 2018 |
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