Loratadine Allergy Relief
NDC 37808-529, Loratadine, tablet, from HEB.
- Product NDC
- 37808-529
- Status
- Listed
- Labeler
- HEB
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA076134
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/37808-529 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LORATADINE10 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 37808-529-01 | 37808052901 | 100 TABLET in 1 BOTTLE (37808-529-01) |
| 37808-529-11 | 37808052911 | 1 BLISTER PACK in 1 CARTON (37808-529-11) / 10 TABLET in 1 BLISTER PACK |
| 37808-529-31 | 37808052931 | 30 BLISTER PACK in 1 CARTON (37808-529-31) / 1 TABLET in 1 BLISTER PACK |
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 37808-529 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/37808-529 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 37808-529. 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.