All Day Allergy Relief
- Product NDC
- 83324-147
- 11-digit product format
- 833240147
- Labeler code
- 83324
- Product ID
- 83324-147_c9df3e7d-93f3-491d-ac43-6d8cbc5d457d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2024-07-31
- 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 |
|---|
| 83324-147-10 | 83324014710 | 10 BLISTER PACK in 1 CARTON (83324-147-10) / 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2024-07-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | QUALITY CHOICE (Chain Drug Marketing Association) | 2024-05-16 | HUMAN OTC DRUG LABEL | 2 |