PHENOBARBITAL
NDC 70752-162, PHENOBARBITAL, tablet, from QUAGEN PHARMACEUTICALS LLC.
- Product NDC
- 70752-162
- Status
- Listed
- Labeler
- QUAGEN PHARMACEUTICALS LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/70752-162 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENOBARBITAL32.4 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70752-162-10 | 70752016210 | 100 TABLET in 1 BOTTLE (70752-162-10) |
| 70752-162-11 | 70752016211 | 1000 TABLET in 1 BOTTLE (70752-162-11) |
| 70752-162-14 | 70752016214 | 500 TABLET in 1 BOTTLE (70752-162-14) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7e6853a4-478d-40e3-b041-4cff02a74c8c
Use it
Look up 70752-162 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70752-162 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70752-162. 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.