Claritin, CVP
- Product NDC
- 66715-6532
- 11-digit product format
- 667156532
- Labeler code
- 66715
- Product ID
- 66715-6532_f71dd792-11e7-0bfd-e053-6294a90ab948
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lil' Drug Store Products, Inc
- Application
- NDA019658
- Marketing category
- NDA
- Marketing start
- 2017-08-25
- 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 |
|---|
| 66715-6532-1 | 66715653201 | 1 POUCH in 1 CARTON (66715-6532-1) / 1 TABLET in 1 POUCH | 1 pouch | 2017-08-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Claritin ® Antihistamine | Lil' Drug Store Products, Inc | 2023-03-17 | HUMAN OTC DRUG LABEL | 8 |