CAPTOPRIL
- Product NDC
- 69158-005
- 11-digit product format
- 691580005
- Labeler code
- 69158
- Product ID
- 69158-005_baeb6724-4be7-43cb-9271-a4ceb28bcefb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CAPTOPRIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- GLENVIEW PHARMA INC.
- Application
- ANDA074532
- Marketing category
- ANDA
- Marketing start
- 1997-03-28
- Marketing end
- 0000-00-00
- Substance
- CAPTOPRIL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69158-005-00 | CAPTOPRIL | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69158-005 | CAPTOPRIL TABLET [GLENVIEW PHARMA INC.] | 3 | Legacy NDC, 1 package rows | 20140910_8c6678fe-0da2-4f20-bacf-321e37e5799d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69158-005-00 | 69158000500 | 100 in 1 BOTTLE | Historical |