Loratadine
- Product NDC
- 68071-3203
- 11-digit product format
- 680713203
- Labeler code
- 68071
- Product ID
- 68071-3203_4f450c60-fadd-4b9a-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2003-01-21
- 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