All Day Allergy
- Product NDC
- 30142-458
- 11-digit product format
- 301420458
- Labeler code
- 30142
- Product ID
- 30142-458_c5a9ba6f-317d-4652-b0b2-3bcd867060f2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA078336
- Marketing category
- ANDA
- Marketing start
- 2008-01-08
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-458-06 | 30142045806 | 1 BOTTLE in 1 CARTON (30142-458-06) > 70 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-10-02 | 0000-00-00 | No | No | Current |
| 30142-458-39 | 30142045839 | 1 BOTTLE in 1 CARTON (30142-458-39) > 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2008-09-13 | 0000-00-00 | No | No | Current |
| 30142-458-49 | 30142045849 | 1 BOTTLE in 1 CARTON (30142-458-49) > 40 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2014-04-03 | 0000-00-00 | No | No | Current |
| 30142-458-66 | 30142045866 | 14 BLISTER PACK in 1 CARTON (30142-458-66) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 14 blister pack | 2008-01-08 | 0000-00-00 | No | No | Current |
| 30142-458-88 | 30142045888 | 1 BOTTLE in 1 CARTON (30142-458-88) > 365 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-04-19 | 0000-00-00 | No | No | Current |
| 30142-458-92 | 30142045892 | 2 BOTTLE in 1 CARTON (30142-458-92) > 70 TABLET, FILM COATED in 1 BOTTLE | 2 bottle | 2018-01-15 | 0000-00-00 | No | No | Current |