NDC 71205-207 – Cetirizine hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71205-207
Product details
- Brand name
- Cetirizine hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078336
- Marketed since
- December 27, 2007
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-207-06 | 6 TABLET in 1 BOTTLE (71205-207-06) | Sep 1, 2019 |
| 71205-207-10 | 10 TABLET in 1 BOTTLE (71205-207-10) | Aug 1, 2019 |
| 71205-207-15 | 15 TABLET in 1 BOTTLE (71205-207-15) | Oct 1, 2019 |
| 71205-207-30 | 30 TABLET in 1 BOTTLE (71205-207-30) | Jan 1, 2019 |
| 71205-207-60 | 60 TABLET in 1 BOTTLE (71205-207-60) | Jan 1, 2019 |
| 71205-207-90 | 90 TABLET in 1 BOTTLE (71205-207-90) | Jan 1, 2019 |
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