All Day Allergy Relief
- Product NDC
- 63868-432
- 11-digit product format
- 638680432
- Labeler code
- 63868
- Product ID
- 63868-432_cee35bd7-dd9c-42b0-81ab-00fbc479f884
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- ANDA207235
- Marketing category
- ANDA
- Marketing start
- 2018-06-30
- Marketing end
- 2024-02-23
- 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 |
|---|
| 63868-432-25 | 63868043225 | 1 BOTTLE in 1 BOX (63868-432-25) > 25 CAPSULE in 1 BOTTLE | 1 bottle | 2018-06-30 | 0000-00-00 | No | No | Current |