Desmopressin Acetate
NDC 68682-342, Desmopressin Acetate, solution, from Oceanside Pharmaceuticals.
- Product NDC
- 68682-342
- Status
- Listed
- Labeler
- Oceanside Pharmaceuticals
- Dosage form
- SOLUTION
- Route
- NASAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA074830
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68682-342 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DESMOPRESSIN ACETATE.1 mg/mL
Pharmacologic classes
Factor VIII Activator [EPC]; Increased Coagulation Factor VIII Activity [PE]; Increased Coagulation Factor VIII Concentration [PE]; Vasopressin Analog [EPC]; Vasopressins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68682-342-05 | 68682034205 | 1 BOTTLE, PUMP in 1 CARTON (68682-342-05) / 5 mL in 1 BOTTLE, PUMP |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/8034989a-45f5-436b-8b1f-42108ee2a21a
Use it
Look up 68682-342 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68682-342 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68682-342. 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.