Loratadine
- Product NDC
- 50090-7066
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076301
- Marketing category
- ANDA
- Substance
- LORATADINE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-7066-4 | 1 BOTTLE in 1 CARTON (50090-7066-4) / 30 TABLET in 1 BOTTLE | 2024-01-18 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Major Pharmaceuticals Allergy Drug Facts | A-S Medication Solutions | 2025-11-06 | HUMAN OTC DRUG LABEL | 5 |
| Major Pharmaceuticals Allergy Drug Facts | A-S Medication Solutions | 2024-08-21 | HUMAN OTC DRUG LABEL | 3 |