Fosinopril Sodium
- Product NDC
- 50090-2977
- 11-digit product format
- 500902977
- Labeler code
- 50090
- Product ID
- 50090-2977_8f99a421-7303-41b5-bde9-f9beb408fcf8
- 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
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fosinopril Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FOSINOPRIL SODIUM | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NW2RTH6T2N |
| Rxcui | 857169, 857187 |
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 |
|---|
| 50090-2977-0 | Fosinopril Sodium | 30 in 1 BOTTLE | TABLET | 30 | | 19 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2977 | FOSINOPRIL SODIUM (FOSINOPRIL) TABLET [A-S MEDICATION SOLUTIONS] | 19 | Current NDC, Legacy NDC, 1 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 | Sample | Exclude flag | Status |
|---|
| 50090-2977-0 | 50090297700 | 30 TABLET in 1 BOTTLE (50090-2977-0) | 30 tablet | 2017-04-18 | No | No | Historical |