all day allergy d
- Product NDC
- 30142-176
- 11-digit product format
- 301420176
- Labeler code
- 30142
- Product ID
- 30142-176_19a2309d-30f4-463f-916e-55f579ed60fb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl, Pseudoephedrine HCl
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA077170
- Marketing category
- ANDA
- Marketing start
- 2014-02-19
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 30142-176-62 | 30142017662 | 12 BLISTER PACK in 1 CARTON (30142-176-62) > 2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 12 blister pack | 2014-02-19 | 0000-00-00 | No | No | Current |