Fosinopril Sodium
- Product NDC
- 50090-2500
- 11-digit product format
- 500902500
- Labeler code
- 50090
- Product ID
- 50090-2500_45bd946b-2ae5-4ba5-8aee-46f8efe3fa1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2016-06-16
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 50090-2500-0 | 2023-02-06 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
| 50090-2500-1 | 2023-02-06 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
| 50090-2500-0 | 2023-01-30 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
| 50090-2500-1 | 2023-01-30 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
| 50090-2500-0 | 2020-10-01 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
| 50090-2500-1 | 2020-10-01 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
| 50090-2500-0 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
| 50090-2500-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-3826-f424-e053-dadaa90a57ce | FOSINOPRILSODIUM TABLETS, USP 10mg, 20mg and 40mg Rx Only |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2500-0 | Fosinopril Sodium | 30 in 1 BOTTLE | TABLET | 30 | | 19 |
| 50090-2500-1 | Fosinopril Sodium | 90 in 1 BOTTLE | TABLET | 90 | | 19 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2500 | FOSINOPRIL SODIUM (FOSINOPRIL) TABLET [A-S MEDICATION SOLUTIONS] | 19 | Legacy NDC, 2 package rows | 20230219_880e5bf4-ced8-4765-a5c2-2361fd06ed9c.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 |
|---|
| 50090-2500-0 | 50090250000 | 30 TABLET in 1 BOTTLE (50090-2500-0) | 30 tablet | 2016-10-13 | 0000-00-00 | No | No | Current |
| 50090-2500-1 | 50090250001 | 90 TABLET in 1 BOTTLE (50090-2500-1) | 90 tablet | 2018-07-12 | 0000-00-00 | No | No | Current |