NDC 41163-458 – Equaline all day allergy
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC41163-458
Product details
- Brand name
- Equaline all day allergy
- Generic name
- Cetirizine Hydrochloride
- Labeler
- United Natural Foods, Inc. dba UNFI
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078336
- Marketed since
- January 23, 2008
- 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 Equaline all day allergy →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 41163-458-39 | 1 BOTTLE in 1 CARTON (41163-458-39) / 30 TABLET, FILM COATED in 1 BOTTLE | Nov 3, 2008 |
| 41163-458-66 | 14 BLISTER PACK in 1 CARTON (41163-458-66) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Jan 23, 2008 |
| 41163-458-72 | 1 BOTTLE in 1 CARTON (41163-458-72) / 60 TABLET, FILM COATED in 1 BOTTLE | Sep 9, 2009 |
Recalls mentioning this NDC
- D-0525-2016 Dec 30, 2015 · Class III
Failed Impurity/Degradations Specifications; impurity identified as cetirizine monosaccharide ester