NDC 71205-709 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-709
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride Tablets
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078343
- Marketed since
- December 17, 2018
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-709-00 | 100 TABLET, FILM COATED in 1 BOTTLE (71205-709-00) | Jul 8, 2025 |
| 71205-709-06 | 6 TABLET, FILM COATED in 1 BOTTLE (71205-709-06) | Oct 31, 2022 |
| 71205-709-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-709-10) | Oct 31, 2022 |
| 71205-709-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-709-20) | Mar 4, 2026 |
| 71205-709-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-709-30) | Oct 31, 2022 |
| 71205-709-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-709-90) | Oct 31, 2022 |
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