NDC 43598-811 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC43598-811
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride Tablets
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078343
- Marketed since
- December 17, 2018
- 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 |
|---|---|---|
| 43598-811-05 | 1 BOTTLE in 1 CARTON (43598-811-05) / 500 TABLET, FILM COATED in 1 BOTTLE | Dec 17, 2018 |
| 43598-811-12 | 100 TABLET, FILM COATED in 1 BOTTLE (43598-811-12) | Sep 3, 2019 |
| 43598-811-13 | 300 TABLET, FILM COATED in 1 BOTTLE (43598-811-13) | Sep 3, 2019 |
| 43598-811-15 | 500 TABLET, FILM COATED in 1 BOTTLE (43598-811-15) | Sep 3, 2019 |
| 43598-811-30 | 1 BOTTLE in 1 CARTON (43598-811-30) / 300 TABLET, FILM COATED in 1 BOTTLE | Dec 17, 2018 |
| 43598-811-90 | 1 BOTTLE in 1 CARTON (43598-811-90) / 90 TABLET, FILM COATED in 1 BOTTLE | Dec 17, 2018 |
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