Nuvicare-Allergy Relief Loratadine Tablets, 10 mg
- Product NDC
- 84324-027
- 11-digit product format
- 843240027
- Labeler code
- 84324
- Product ID
- 84324-027_042dab86-b69d-4b03-bd6a-539232ef56f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NUVICARE LLC
- Application
- ANDA214684
- Marketing category
- ANDA
- Marketing start
- 2025-07-01
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nuvicare-Allergy Relief Loratadine Tablets, 10 mg
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LORATADINE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7AJO3BO7QN |
| Rxcui | 311372 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84324-027-01 | Nuvicare-Allergy Relief Loratadine Tablets, 10 mg | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84324-027-01 | 84324002701 | 100 TABLET in 1 BOTTLE (84324-027-01) | 100 tablet | 2025-07-01 | No | No | Current |