NDC 42507-458 – All Day Allergy
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC42507-458
Product details
- Brand name
- All Day Allergy
- Generic name
- Cetirizine Hydrochloride
- Labeler
- HyVee Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078336
- Marketed since
- August 28, 1997
- 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 All day allergy →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 42507-458-39 | 1 BOTTLE in 1 CARTON (42507-458-39) / 30 TABLET, FILM COATED in 1 BOTTLE (42507-458-30) | Dec 8, 2008 |
| 42507-458-72 | 1 BOTTLE in 1 CARTON (42507-458-72) / 60 TABLET, FILM COATED in 1 BOTTLE (42507-458-60) | Aug 28, 1997 |
| 42507-458-75 | 1 BOTTLE in 1 CARTON (42507-458-75) / 90 TABLET, FILM COATED in 1 BOTTLE (42507-458-90) | Jun 27, 2009 |
| 42507-458-87 | 1 BOTTLE in 1 CARTON (42507-458-87) / 300 TABLET, FILM COATED in 1 BOTTLE (42507-458-00) | Jan 28, 2026 |
| 42507-458-95 | 1 BOTTLE in 1 CARTON (42507-458-95) / 45 TABLET, FILM COATED in 1 BOTTLE (42507-458-45) | Jan 19, 2009 |
Recalls mentioning this NDC
- D-0525-2016 Dec 30, 2015 · Class III
Failed Impurity/Degradations Specifications; impurity identified as cetirizine monosaccharide ester
Other All day allergy products
- 11822-1002 Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Rite Aid Corporation
- 41520-212 Cetirizine Hydrochloride 10 mg/1 · Capsule, Liquid Filled · Care One (American Sales Company)
- 41163-219 Cetirizine Hydrochloride 10 mg/1 · Capsule · SUPERVALU INC
- 79903-084 Cetirizine Hydrochloride 10 mg/1 · Capsule · WALMART INC. (see also Equate)