Cetirizine Hydrochloride 55111-0351
Product NDC
55111-0351- Manufacturer
- Dr.reddy's Laboratories Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- January 15, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA078343
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(8)
1 BOTTLE in 1 CARTON (55111-351-04) / 120 TABLET, FILM COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (55111-351-30) / 30 TABLET, FILM COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (55111-351-45) / 45 TABLET, FILM COATED in 1 BOTTLE
2 BOTTLE in 1 CARTON (55111-351-47) / 175 TABLET, FILM COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (55111-351-51) / 75 TABLET, FILM COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (55111-351-60) / 60 TABLET, FILM COATED in 1 BOTTLE
2 BLISTER PACK in 1 CARTON (55111-351-74) / 7 TABLET, FILM COATED in 1 BLISTER PACK
1 BOTTLE in 1 CARTON (55111-351-90) / 90 TABLET, FILM COATED in 1 BOTTLE