All Day Allergy-D
- Product NDC
- 0113-2176
- 11-digit product format
- 001132176
- Labeler code
- 0113
- Product ID
- 0113-2176_472d5e74-fd17-4583-b95b-de985e37c07b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl, Pseudoephedrine HCl
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA077170
- Marketing category
- ANDA
- Marketing start
- 2011-09-06
- 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 |
|---|
| 0113-2176-53 | 00113217653 | 2 BLISTER PACK in 1 CARTON (0113-2176-53) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2013-09-26 | 0000-00-00 | No | No | Current |
| 0113-2176-62 | 00113217662 | 4 BLISTER PACK in 1 CARTON (0113-2176-62) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2011-09-06 | 0000-00-00 | No | No | Current |