Ramipril
- Product NDC
- 31722-274
- 11-digit product format
- 317220274
- Labeler code
- 31722
- Product ID
- 31722-274_235c5540-0408-43d8-80bb-b8e31ed815e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ramipril
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals
- Application
- ANDA078745
- Marketing category
- ANDA
- Marketing start
- 2011-01-01
- Marketing end
- 0000-00-00
- Substance
- RAMIPRIL
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-274 | RAMIPRIL CAPSULE [CAMBER PHARMACEUTICALS] | 2 | Legacy NDC | 20110829_a1064f8a-90f5-4c66-9f3c-cd5f17260eb9.zip |