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NDC 21130-644, cetirizine hydrochloride, pseudoephedrine hydrochloride, tablet, film coated, extended release, from Safeway.
- Product NDC
- 21130-644
- Status
- Listed
- Labeler
- Safeway
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA210719
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/21130-644 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CETIRIZINE HYDROCHLORIDE5 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE120 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA]; Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]; alpha-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 21130-644-62 | 21130064462 | 24 BLISTER PACK in 1 CARTON (21130-644-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE 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 21130-644 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/21130-644 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 21130-644. 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.