Allergy and congestion relief
- Product NDC
- 30142-013
- 11-digit product format
- 301420013
- Labeler code
- 30142
- Product ID
- 30142-013_e27304da-de30-4eda-9025-39672d7b55a7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine, Pseudoephedrine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA076050
- Marketing category
- ANDA
- Marketing start
- 2012-04-06
- Marketing end
- 0000-00-00
- Substance
- LORATADINE; PSEUDOEPHEDRINE SULFATE
- Active strength
- 5 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#