Propranolol Hydrochloride
NDC 68071-5071, propranolol hydrochloride, tablet, from NuCare Pharmaceuticals,Inc..
- Product NDC
- 68071-5071
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA070221
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5071 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PROPRANOLOL HYDROCHLORIDE80 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-5071-1 | 68071507101 | 100 TABLET in 1 BOTTLE (68071-5071-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/933f792f-341f-4d71-e053-2a95a90ad341
Use it
Look up 68071-5071 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5071 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-5071. 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.