Claritin
- Product NDC
- 70264-030
- 11-digit product format
- 702640030
- Labeler code
- 70264
- Product ID
- 70264-030_43c8f3f3-5cc5-a286-e063-6294a90a6192
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- R J General Corporation
- Application
- NDA019658
- Marketing category
- NDA
- Marketing start
- 2021-03-01
- 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
- Claritin
- 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 | 206805, 311372 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70264-030-01 | Claritin | 1 in 1 POUCH | TABLET | 1 | | 4 |
| 70264-030-01 | Claritin | 25 in 1 CARTON | TABLET | 25 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70264-030 | CLARITIN (LORATADINE) TABLET [R J GENERAL CORPORATION] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241112_a34e8cb7-4fdf-45be-b288-45d93eef6220.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70264-030-01 | 70264003001 | 25 POUCH in 1 CARTON (70264-030-01) / 1 TABLET in 1 POUCH | 25 pouch | 2022-12-26 | 0000-00-00 | No | No | Current |