All Day Allergy
- Product NDC
- 63868-139
- 11-digit product format
- 638680139
- Labeler code
- 63868
- Product ID
- 63868-139_d357d8bf-bd25-49d7-8b06-b20f2738914c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- NDA022429
- Marketing category
- NDA
- Marketing start
- 2016-04-30
- Marketing end
- 2024-05-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-139-25 | 63868013925 | 1 BOTTLE, PLASTIC in 1 PACKAGE (63868-139-25) > 25 CAPSULE in 1 BOTTLE, PLASTIC | 2016-04-30 | 0000-00-00 | No | No | Current |