24 hour allergy
- Product NDC
- 79481-0981
- 11-digit product format
- 794810981
- Labeler code
- 79481
- Product ID
- 79481-0981_8d69bdb3-957b-4af3-9255-79dda46dd5fd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- cetirizine hydrochloride
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Meijer, Inc.
- Application
- ANDA213105
- Marketing category
- ANDA
- Marketing start
- 2022-03-08
- 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 |
|---|
| 79481-0981-0 | 79481098100 | 1 BOTTLE in 1 PACKAGE (79481-0981-0) / 25 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2022-03-08 | No | No | Historical |