Loratadine
- Product NDC
- 0781-5077
- 11-digit product format
- 007815077
- Labeler code
- 0781
- Product ID
- 0781-5077_7b2c3c36-bf13-46b7-908c-949672ebf806
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2003-01-21
- Marketing end
- 2020-09-30
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0781-5077-01 | EA - Each | 0781-5077 | ee2bd65b-3fef-4be8-badd-bf30aea9e7c9 | 1 | 2012-07-24 |
| 0781-5077-64 | EA - Each | 0781-5077 | d1533bfe-0d09-41a8-b3de-70ebebf3c12b | 1 | 2012-07-24 |
| 0781-5077-76 | EA - Each | 0781-5077 | 7f0bca63-8292-4908-b293-10884106fc88 | 1 | 2013-02-11 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 311372 | loratadine 10 MG 24HR Oral Tablet | PSN | 59905847-f1a5-0dee-e053-2a91aa0aafed | 1 |
| 311372 | loratadine 10 MG Oral Tablet | SCD | 59905847-f1a5-0dee-e053-2a91aa0aafed | 1 |
| 311372 | loratadine 10 MG 24 HR Oral Tablet | SY | 59905847-f1a5-0dee-e053-2a91aa0aafed | 1 |