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- Product NDC
- 11673-555
- 11-digit product format
- 116730555
- Labeler code
- 11673
- Product ID
- 11673-555_b3ca5e87-2542-4c54-8090-38bf191522fa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl, Pseudoephedrine HCl
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA077170
- Marketing category
- ANDA
- Marketing start
- 2015-03-12
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record