allergy relief
- Product NDC
- 30142-446
- 11-digit product format
- 301420446
- Labeler code
- 30142
- Product ID
- 30142-446_cea1ba0b-2f40-406a-80ab-ebabc535f406
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA076011
- Marketing category
- ANDA
- Marketing start
- 2021-06-04
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 30142-446-65 | 30142044665 | 30 BLISTER PACK in 1 CARTON (30142-446-65) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 30 blister pack | 2021-06-04 | No | No | Historical |