Fexofenadine HCL
NDC 72789-196, Fexofenadine HCL, tablet, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 72789-196
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA204097
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72789-196 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FEXOFENADINE HYDROCHLORIDE180 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72789-196-10 | 72789019610 | 10 TABLET in 1 BOTTLE, PLASTIC (72789-196-10) |
| 72789-196-30 | 72789019630 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-196-30) |
| 72789-196-90 | 72789019690 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-196-90) |
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 72789-196 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72789-196 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72789-196. 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.