Loratadine
- Product NDC
- 49348-112
- 11-digit product format
- 493480112
- Labeler code
- 49348
- Product ID
- 49348-112_7c9589a4-0219-4c83-a946-266502ad70f5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sunmark
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2016-06-01
- Marketing end
- 2020-10-31
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record