LEADER Loratadine
- Product NDC
- 37205-346
- 11-digit product format
- 372050346
- Labeler code
- 37205
- Product ID
- 37205-346_fe6bc6f0-dfff-49a9-8251-43dfa0a48df2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2003-08-19
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 37205-346-47 | EA - Each | 37205-346 | 86d3780b-e6dc-4a86-ba59-fd81c341a4c9 | 1 | 2013-02-13 |
| 37205-346-52 | EA - Each | 37205-346 | df3c78db-17d8-4973-998a-f2fd5a843f6a | 1 | 2012-07-24 |
| 37205-346-60 | EA - Each | 37205-346 | 0bcff87b-4de1-46f0-a689-8b06d8f68dc9 | 1 | 2012-07-24 |
| 37205-346-65 | EA - Each | 37205-346 | c3b2a5f5-fac4-4014-aa85-ee6a125cac24 | 1 | 2012-07-24 |
| 37205-346-72 | EA - Each | 37205-346 | c8c25625-0cfd-47db-90f9-1e5615bbb7dc | 1 | 2013-02-13 |
| 37205-346-75 | EA - Each | 37205-346 | 4f56ac9e-7944-49b8-8621-5aa05c2c8c32 | 1 | 2013-02-13 |