Equaline All Day Allergy D
- Product NDC
- 41163-176
- 11-digit product format
- 411630176
- Labeler code
- 41163
- Product ID
- 41163-176_00ec28fe-c6c2-498f-9951-07b40f3e52e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl, Pseudoephedrine HCl
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Supervalu Inc
- Application
- ANDA077170
- Marketing category
- ANDA
- Marketing start
- 2008-07-30
- 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 |
|---|
| 41163-176-62 | 41163017662 | 24 BLISTER PACK in 1 CARTON (41163-176-62) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 24 blister pack | 2008-07-30 | 0000-00-00 | No | No | Current |