Cetirizine Hydrochloride
NDC 71205-709, Cetirizine Hydrochloride Tablets, tablet, film coated, from Proficient Rx LP.
- Product NDC
- 71205-709
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA078343
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71205-709 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CETIRIZINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-709-00 | 71205070900 | 100 TABLET, FILM COATED in 1 BOTTLE (71205-709-00) |
| 71205-709-06 | 71205070906 | 6 TABLET, FILM COATED in 1 BOTTLE (71205-709-06) |
| 71205-709-10 | 71205070910 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-709-10) |
| 71205-709-20 | 71205070920 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-709-20) |
| 71205-709-30 | 71205070930 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-709-30) |
| 71205-709-90 | 71205070990 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-709-90) |
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 71205-709 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-709 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-709. 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.