allergy relief
- Product NDC
- 41250-523
- 11-digit product format
- 412500523
- Labeler code
- 41250
- Product ID
- 41250-523_50236ffe-b7d0-4b35-a623-0046684d605c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA076301
- Marketing category
- ANDA
- Marketing start
- 2017-07-12
- 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