Loratadine
- Product NDC
- 35356-881
- 11-digit product format
- 353560881
- Labeler code
- 35356
- Product ID
- 35356-881_868b51bf-d418-4e2e-97a1-55c9699fe27b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076301
- Marketing category
- ANDA
- Marketing start
- 2008-10-15
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record