Loratadine
- Product NDC
- 70518-0325
- 11-digit product format
- 705180325
- Labeler code
- 70518
- Product ID
- 70518-0325_9b2549f3-242a-c7fe-e053-2a95a90ad6aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2017-03-16
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record