good sense allergy relief
- Product NDC
- 50090-7051
- 11-digit product format
- 500907051
- Labeler code
- 50090
- Product ID
- 50090-7051_2607fca8-caab-4e8e-b3cd-3c32d17d2eb0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076301
- Marketing category
- ANDA
- Marketing start
- 2004-09-21
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 50090-7051-0 | 50090705100 | 8 BOTTLE in 1 CASE (50090-7051-0) / 90 TABLET in 1 BOTTLE | 8 bottle | 2024-01-15 | No | No | Historical |