Ramipril
- Product NDC
- 60687-332
- 11-digit product format
- 606870332
- Labeler code
- 60687
- Product ID
- 60687-332_8d2e27e5-304f-b151-e053-2995a90a3f32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078832
- Marketing category
- ANDA
- Marketing start
- 2017-10-13
- Marketing end
- 2019-08-31
- Substance
- RAMIPRIL
- Active strength
- 3 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record