Loratadine
NDC 73581-229, Loratadine, tablet, from YYBA CORP.
- Product NDC
- 73581-229
- Status
- Listed
- Labeler
- YYBA CORP
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA208314
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/73581-229 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LORATADINE10 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 73581-229-01 | 73581022901 | 1 BOTTLE in 1 CARTON (73581-229-01) / 100 TABLET in 1 BOTTLE |
| 73581-229-03 | 73581022903 | 1 BOTTLE in 1 CARTON (73581-229-03) / 365 TABLET in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 73581-229 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/73581-229 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 73581-229. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.