Guaifenesin and Pseudoephedrine HCl
NDC 11822-0046, Guaifenesin and Pseudoephedrine HCL, tablet, extended release, from Rite Aid Corporation.
- Product NDC
- 11822-0046
- Status
- Listed
- Labeler
- Rite Aid Corporation
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA208369
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/11822-0046 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GUAIFENESIN600 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE60 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA]; Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]; alpha-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 11822-0046-1 | 11822004601 | 1 BLISTER PACK in 1 CARTON (11822-0046-1) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| 11822-0046-2 | 11822004602 | 2 BLISTER PACK in 1 CARTON (11822-0046-2) / 18 TABLET, 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 11822-0046 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/11822-0046 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 11822-0046. 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.