LORATADINE
- Product NDC
- 0904-5793
- 11-digit product format
- 009045793
- Labeler code
- 0904
- Product ID
- 0904-5793_61657bee-6af6-47f7-8f97-a18f4530d133
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA076471
- Marketing category
- ANDA
- Marketing start
- 2016-06-22
- Marketing end
- 2020-06-30
- 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 |
|---|---|---|---|---|---|
| 0904-5793-61 | EA - Each | 0904-5793 | b27366a2-341e-4cd1-a9b4-e18c31048f20 | 1 | 2016-07-19 |