Allergy Relief
- Product NDC
- 50090-4266
- 11-digit product format
- 500904266
- Labeler code
- 50090
- Product ID
- 50090-4266_6aafc9be-454b-4b5c-b2c8-ca69b3f4dc00
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2018-12-31
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7AJO3BO7QN | LORATADINE | 79794-75-5 | LORATADINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4266-0 | 50090426600 | 30 TABLET in 1 BOTTLE (50090-4266-0) | 30 tablet | 2019-04-17 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | A-S Medication Solutions | 2021-03-01 | HUMAN OTC DRUG LABEL | 1 |