Ramipril
- Product NDC
- 16729-153
- 11-digit product format
- 167290153
- Labeler code
- 16729
- Product ID
- 16729-153_c2d4669a-76a4-4b64-e053-2a95a90a036d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Accord Healthcare Inc.
- Application
- ANDA202392
- Marketing category
- ANDA
- Marketing start
- 2015-02-12
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 16729-153-01 | 16729015301 | 100 CAPSULE in 1 BOTTLE (16729-153-01) | 100 capsule | 2015-02-12 | 0000-00-00 | No | No | Current |
| 16729-153-16 | 16729015316 | 500 CAPSULE in 1 BOTTLE (16729-153-16) | 500 capsule | 2015-02-12 | 0000-00-00 | No | No | Current |