Ramipril
- Product NDC
- 50090-2169
- 11-digit product format
- 500902169
- Labeler code
- 50090
- Product ID
- 50090-2169_ea67929b-19ad-471e-9a2b-03aa251efed9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202392
- Marketing category
- ANDA
- Marketing start
- 2015-02-12
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record