Fosinopril Sodium
- Product NDC
- 63629-5279
- 11-digit product format
- 636295279
- Labeler code
- 63629
- Product ID
- 63629-5279_80189e37-1fe5-4d28-98dc-bbd20051a023
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2007-09-17
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 90aa3f6a-97f0-be7e-d25b-b26d56ae287e | Product name | 3 | 20201015 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-5279-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c54d-f424-e053-dadaa90a57ce | FOSINOPRIL SODIUM TABLETS 10 mg, 20 mg and 40 mg Rx only |
| 63629-5279-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c54d-f424-e053-dadaa90a57ce | FOSINOPRIL SODIUM TABLETS 10 mg, 20 mg and 40 mg Rx only |
| 63629-5279-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c54d-f424-e053-dadaa90a57ce | FOSINOPRIL SODIUM TABLETS 10 mg, 20 mg and 40 mg Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63629-5279-1 | Fosinopril Sodium | 30 in 1 BOTTLE | TABLET | 30 | 1001 | |
| 63629-5279-2 | Fosinopril Sodium | 90 in 1 BOTTLE | TABLET | 90 | 1001 | |
| 63629-5279-3 | Fosinopril Sodium | 60 in 1 BOTTLE | TABLET | 60 | 1001 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FOSINOPRIL SODIUM | ACTIVE INGREDIENT | NW2RTH6T2N | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1000 | |
| FOSINOPRILAT | ACTIVE MOIETY | S312EY6ZT8 | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1000 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1000 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1000 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1000 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1000 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1000 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63629-5279 | FOSINOPRIL SODIUM TABLET [BRYANT RANCH PREPACK] | 1001 | Legacy NDC, 3 package rows | 20160630_835c13d6-c3af-498d-9011-325d34006daf.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 857169 | fosinopril sodium 10 MG Oral Tablet | PSN | 835c13d6-c3af-498d-9011-325d34006daf | 1001 |
| 857169 | fosinopril sodium 10 MG Oral Tablet | SCD | 835c13d6-c3af-498d-9011-325d34006daf | 1001 |
| 857169 | FNP Sodium 10 MG Oral Tablet | SY | 835c13d6-c3af-498d-9011-325d34006daf | 1001 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 63629-5279-1 | 63629527901 | 30 in 1 BOTTLE | Historical |
| 63629-5279-2 | 63629527902 | 90 in 1 BOTTLE | Historical |
| 63629-5279-3 | 63629527903 | 60 in 1 BOTTLE | Historical |