Loratadine
- Product NDC
- 0179-8317
- 11-digit product format
- 001798317
- Labeler code
- 0179
- Product ID
- 0179-8317_7b098b92-2a83-569a-e053-2991aa0aae2d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kaiser Foundation Hospitals
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2011-02-23
- Marketing end
- 2020-08-31
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record