Claritin
- Product NDC
- 73097-005
- 11-digit product format
- 730970005
- Labeler code
- 73097
- Product ID
- 73097-005_8d5a2d85-0f6f-9274-e053-2a95a90a0376
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Savings Distributors LLC
- Application
- NDA019658
- Marketing category
- NDA
- Marketing start
- 2019-07-03
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73097-005 | CLARITIN (LORATADINE) TABLET [SAVINGS DISTRIBUTORS LLC] | 1 | Legacy NDC, 6 package rows | 20190711_8d59f35f-9b84-def8-e053-2995a90aaba7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 73097-005-01 | 73097000501 | 1 in 1 CARTON | Historical |
| 73097-005-20 | 73097000520 | 20 in 1 CARTON | Historical |
| 73097-005-25 | 73097000525 | 25 in 1 CARTON | Historical |