Captopril
- Product NDC
- 67296-0678
- 11-digit product format
- 672960678
- Labeler code
- 67296
- Product ID
- 67296-0678_0188b189-ceb0-492d-a252-f00de0f616a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- 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 |
|---|
| 67296-0678-1 | Captopril | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0678 | CAPTOPRIL TABLET [REDPHARM DRUG INC.] | 1 | Legacy NDC, 1 package rows | 20110824_6bb32e86-c704-42cf-bf36-6b556cd41602.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0678-1 | 67296067801 | 60 in 1 BOTTLE | Historical |