Loratadine
- Product NDC
- 62011-0258
- 11-digit product format
- 620110258
- Labeler code
- 62011
- Product ID
- 62011-0258_450c38da-a38f-4bce-88d3-dd364bc005c9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HealthMart
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- Marketing end
- 2020-10-31
- 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 |
|---|---|---|---|---|---|
| 62011-0258-1 | EA - Each | 62011-0258 | e745e2d8-02a7-4322-ba8b-b279eb1e0d05 | 1 | 2017-11-06 |
| 62011-0258-2 | EA - Each | 62011-0258 | 7a2ab27b-bd3f-4e5e-acac-f21848fe7c4e | 1 | 2017-11-06 |
| 62011-0258-3 | EA - Each | 62011-0258 | e6d4c6a3-fd75-4b1d-ade8-a6853fbb175f | 1 | 2017-11-06 |
| 62011-0258-4 | EA - Each | 62011-0258 | 7043f178-7d31-4048-8bc5-a46fe035ecf1 | 1 | 2017-06-15 |