Loratadine
- Product NDC
- 49348-112
- 11-digit product format
- 493480112
- Labeler code
- 49348
- Product ID
- 49348-112_7c9589a4-0219-4c83-a946-266502ad70f5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sunmark
- 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 |
|---|---|---|---|---|---|
| 49348-112-01 | EA - Each | 49348-112 | 094763c9-af9e-4ae8-99d2-e3a98c13f914 | 1 | 2017-11-06 |
| 49348-112-13 | EA - Each | 49348-112 | 03026ae0-9b61-493c-8b78-3fb6ac8e0e11 | 1 | 2017-11-06 |
| 49348-112-44 | EA - Each | 49348-112 | 0674719c-d55f-4905-aa4f-db462a82b63d | 1 | 2017-11-06 |