captopril
- Product NDC
- 50090-5964
- 11-digit product format
- 500905964
- Labeler code
- 50090
- Product ID
- 50090-5964_c2807653-6e54-4d6a-a3fc-44a72f4a0f10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074677
- Marketing category
- ANDA
- Marketing start
- 2019-08-20
- Marketing end
- 0000-00-00
- Substance
- CAPTOPRIL
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50090-5964-3 | captopril | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5964 | CAPTOPRIL TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20220921_00871911-8c79-433c-87d5-181f4c973d5b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5964-3 | 50090596403 | 60 TABLET in 1 BOTTLE (50090-5964-3) | 60 tablet | 2022-04-21 | 0000-00-00 | No | No | Current |