Captopril
- Product NDC
- 68151-0050
- 11-digit product format
- 681510050
- Labeler code
- 68151
- Product ID
- 68151-0050_6f8d2952-d458-46c2-8157-b0598b1a6d02
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA074505
- Marketing category
- ANDA
- Marketing start
- 1996-02-13
- 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 |
|---|
| 68151-0050-8 | Captopril | 1 in 1 CUP | TABLET | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-0050 | CAPTOPRIL TABLET [CARILION MATERIALS MANAGEMENT] | 7 | Legacy NDC, 1 package rows | 20171227_3aa39c24-1f08-4b52-b30a-a158a742db0a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-0050-8 | 68151005008 | 1 in 1 CUP | Historical |