Allergy Relief
- Product NDC
- 0363-1794
- 11-digit product format
- 003631794
- Labeler code
- 0363
- Product ID
- 0363-1794_08332210-6c16-be1e-e063-6394a90a0bbe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- WALGREENS
- Application
- ANDA078933
- Marketing category
- ANDA
- Marketing start
- 2023-10-25
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 64O047KTOA | CETIRIZINE HYDROCHLORIDE | 83881-52-1 | CETIRIZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-1794-38 | 00363179438 | 1 BLISTER PACK in 1 CARTON (0363-1794-38) / 5 TABLET in 1 BLISTER PACK | 1 blister pack | 2023-10-25 | No | No | Historical |
| 0363-1794-46 | 00363179446 | 1 BLISTER PACK in 1 CARTON (0363-1794-46) / 14 TABLET in 1 BLISTER PACK | 1 blister pack | 2023-10-25 | No | No | Historical |