Allergy relief-D
- Product NDC
- 49035-982
- 11-digit product format
- 490350982
- Labeler code
- 49035
- Product ID
- 49035-982_ef4fc264-bf2e-404d-95a0-ff92ed0bc347
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- EQUATE (WAL-MART STORES, INC.)
- Application
- ANDA090922
- Marketing category
- ANDA
- Marketing start
- 2019-05-31
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 64O047KTOA | CETIRIZINE HYDROCHLORIDE | 83881-52-1 | CETIRIZINE HYDROCHLORIDE |
| 6V9V2RYJ8N | PSEUDOEPHEDRINE HYDROCHLORIDE | 345-78-8 | PSEUDOEPHEDRINE HYDROCHLORIDE |