Loratadine
- Product NDC
- 50436-3502
- 11-digit product format
- 504363502
- Labeler code
- 50436
- Product ID
- 50436-3502_08c4eeec-7df1-4ac1-8557-46eb0118a02d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record