LORATADINE
- Product NDC
- 70518-1262
- 11-digit product format
- 705181262
- Labeler code
- 70518
- Product ID
- 70518-1262_91131f09-81a2-556b-e053-2995a90ae35e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076471
- Marketing category
- ANDA
- Marketing start
- 2018-06-18
- 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