Loratadine
- Product NDC
- 82501-1580
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Gobrands, Inc
- Application
- ANDA214684
- Marketing category
- ANDA
- Substance
- LORATADINE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 82501-1580-3 | 1 BOTTLE in 1 CARTON (82501-1580-3) / 30 TABLET in 1 BOTTLE | 20220516 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 1d182bd6-ad72-4352-b983-407a48c317f0 | NON-DROWSY 24 HOUR Allergy Relief Loratadine Antihistamine | Gobrands, Inc | 2025-01-25 | HUMAN OTC DRUG LABEL | 5 |