Pseudoephedrine hydrochloride
NDC 51660-204, Pseudoephedrine hydrochloride, tablet, film coated, from Ohm Laboratories Inc..
- Product NDC
- 51660-204
- Status
- Listed
- Labeler
- Ohm Laboratories Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA077442
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51660-204 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PSEUDOEPHEDRINE HYDROCHLORIDE120 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA]; alpha-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51660-204-21 | 51660020421 | 20 TABLET, FILM COATED in 1 BLISTER PACK (51660-204-21) |
| 51660-204-69 | 51660020469 | 10 TABLET, FILM COATED in 1 BLISTER PACK (51660-204-69) |
Linked data
RxNorm, label and prices
Related lookups
NADAC price for package 51660020421
GET /v1/drugs/nadac/51660020421NADAC price for package 51660020469
GET /v1/drugs/nadac/51660020469
Use it
Look up 51660-204 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51660-204 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51660-204. 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.