Fosinopril Sodium
- Product NDC
- 62135-042
- 11-digit product format
- 621350042
- Labeler code
- 62135
- Product ID
- 62135-042_40d2b698-02dc-4589-e063-6394a90afb52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA076483
- Marketing category
- ANDA
- Marketing start
- 2004-04-23
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 20 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NW2RTH6T2N |
| Rxcui | 857169, 857183, 857187 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-042-90 | Fosinopril Sodium | 90 in 1 BOTTLE | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-042 | FOSINOPRIL SODIUM TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20241030_ff1323cc-7ad8-488d-94a7-a11555db78a7.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 |
|---|
| 62135-042-90 | 62135004290 | 90 TABLET in 1 BOTTLE (62135-042-90) | 90 tablet | 2023-06-01 | No | No | Current |