Ramipril
- Product NDC
- 60687-321
- 11-digit product format
- 606870321
- Labeler code
- 60687
- Product ID
- 60687-321_b027a726-c8e0-3d01-e053-2995a90ade49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078832
- Marketing category
- ANDA
- Marketing start
- 2017-09-07
- Marketing end
- 2021-05-31
- Substance
- RAMIPRIL
- Active strength
- 1 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-321-21 | 60687032121 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-321-21) > 1 CAPSULE in 1 BLISTER PACK (60687-321-11) | 30 blister pack | 2017-09-07 | 2021-05-31 | No | No | Current |