Ramipril
- Product NDC
- 70518-1175
- 11-digit product format
- 705181175
- Labeler code
- 70518
- Product ID
- 70518-1175_9088e1c0-a44b-edee-e053-2995a90a0984
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077900
- Marketing category
- ANDA
- Marketing start
- 2018-05-14
- Marketing end
- 0000-00-00
- Substance
- RAMIPRIL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record