NDC 58602-838 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Orally Disintegrating · Oral
Product NDC58602-838
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing category
- ANDA · ANDA213557
- Marketed since
- September 11, 2020
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 58602-838-14 | 11 BLISTER PACK in 1 CARTON (58602-838-14) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74) | Sep 11, 2020 |
| 58602-838-19 | 20 BLISTER PACK in 1 CARTON (58602-838-19) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74) | Jan 28, 2025 |
| 58602-838-75 | 2 BLISTER PACK in 1 CARTON (58602-838-75) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74) | Sep 11, 2020 |
| 58602-838-76 | 4 BLISTER PACK in 1 CARTON (58602-838-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (58602-838-74) | Sep 11, 2020 |
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