Fosinopril Sodium
- Product NDC
- 31722-201
- 11-digit product format
- 317220201
- Labeler code
- 31722
- Product ID
- 31722-201_29914956-c794-4806-b038-f0784b9db3d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmceuticals Inc.
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2007-09-17
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 20 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 |
|---|---|---|---|---|---|
| 31722-201-10 | 2025-04-15 | C162847 | 48780-1 | 960f7f55-ceb4-8e05-e053-dbdaa90a074a | aa425a18-9d34-4b3b-9ef8-fbff79471686 |
| 31722-201-90 | 2025-04-15 | C162847 | 48780-1 | 960f7f55-ceb4-8e05-e053-dbdaa90a074a | aa425a18-9d34-4b3b-9ef8-fbff79471686 |
| 31722-201-10 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-ceb4-8e05-e053-dbdaa90a074a | aa425a18-9d34-4b3b-9ef8-fbff79471686 |
| 31722-201-90 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-ceb4-8e05-e053-dbdaa90a074a | aa425a18-9d34-4b3b-9ef8-fbff79471686 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 31722-201-10 | EA - Each | 31722-201 | 552174b1-48ae-4d09-98bc-e8cf15029f52 | 1 | 2013-02-13 |
| 31722-201-90 | EA - Each | 31722-201 | 018030b1-321d-4b82-b96b-48abf4c17626 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FOSINOPRIL SODIUM | ACTIVE INGREDIENT | NW2RTH6T2N | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 | |
| FOSINOPRILAT | ACTIVE MOIETY | S312EY6ZT8 | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | FOSINOPRIL SODIUM TABLET [UNIT DOSE SERVICES] | 2 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 857183 | fosinopril sodium 20 MG Oral Tablet | PSN | 1cd8aac4-c59a-460d-97d7-ba3b80e0ab82 | 2 |
| 857183 | fosinopril sodium 20 MG Oral Tablet | SCD | 1cd8aac4-c59a-460d-97d7-ba3b80e0ab82 | 2 |
| 857183 | FNP Sodium 20 MG Oral Tablet | SY | 1cd8aac4-c59a-460d-97d7-ba3b80e0ab82 | 2 |