All Day Allergy
- Product NDC
- 62011-0552
- 11-digit product format
- 620110552
- Labeler code
- 62011
- Product ID
- 62011-0552_198ee3d2-27f1-4f9d-92c3-a1e918b264a7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA078780
- Marketing category
- ANDA
- Marketing start
- 2012-02-08
- Marketing end
- 2022-12-30
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 62011-0552-1 | 62011055201 | 1 BLISTER PACK in 1 CARTON (62011-0552-1) > 14 TABLET in 1 BLISTER PACK | 1 blister pack | 2012-02-08 | 2022-12-30 | No | No | Current |