Levocetirizine Dihydrochloride
NDC 71205-210, levocetirizine Dihydrochloride, tablet, film coated, from Proficient Rx LP.
- Product NDC
- 71205-210
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202046
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71205-210 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVOCETIRIZINE DIHYDROCHLORIDE5 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-210-30 | 71205021030 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-210-30) |
| 71205-210-60 | 71205021060 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-210-60) |
| 71205-210-90 | 71205021090 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-210-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f10cfe9a-1884-4a65-b827-8fd781fb75c4
Use it
Look up 71205-210 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-210 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-210. 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.