lisinopril
- Product NDC
- 33358-212
- 11-digit product format
- 333580212
- Labeler code
- 33358
- Product ID
- 33358-212_a4750725-8605-4dd3-a3cf-6eba9d58ae53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RxChange Co.
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL
- 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 |
|---|---|---|---|
| f8f05a6d-f74b-4e9e-ab1c-374d3b4fb820 | Product name | 1 | 20230703 |
| f65307a7-3644-0a09-cdfd-94aae8d3b53e | Product name | 3 | 20210902 |
| 1bdb87cf-9b1f-6a51-5eb7-d182aaffaa3d | Product name | 2 | 20170719 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 33358-212-30 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-392b-f424-e053-dadaa90a57ce | These highlights do not include all the information needed to use Lisinopril Tablets USP safely and effectively. See full prescribing information for Lisinopril Tablets USP Lisinopril Tablets USP, for oral use Initial U.S. Approval: 1988 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 33358-212-30 | lisinopril | 30 in 1 BOTTLE | TABLET | 30 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 33358-212-30 | EA - Each | 33358-212 | db73af70-a413-4b7c-88e6-26f741b29148 | 1 | 2014-12-01 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| LISINOPRIL | ACTIVE INGREDIENT | E7199S1YWR | LISINOPRIL TABLET [RXCHANGE CO.] | 1 | |
| LISINOPRIL ANHYDROUS | ACTIVE MOIETY | 7Q3P4BS2FD | LISINOPRIL TABLET [RXCHANGE CO.] | 1 | |
| CALCIUM PHOSPHATE | INACTIVE INGREDIENT | 97Z1WI3NDX | LISINOPRIL TABLET [RXCHANGE CO.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | LISINOPRIL TABLET [RXCHANGE CO.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | LISINOPRIL TABLET [RXCHANGE CO.] | 1 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | LISINOPRIL TABLET [RXCHANGE CO.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | LISINOPRIL TABLET [RXCHANGE CO.] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 314076 | lisinopril 10 MG Oral Tablet | PSN | fa63e09f-9f95-4c57-9a89-b8d5d3c2a9b4 | 1 |
| 314076 | lisinopril 10 MG Oral Tablet | SCD | fa63e09f-9f95-4c57-9a89-b8d5d3c2a9b4 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 33358-212-30 | 33358021230 | 30 in 1 BOTTLE | Historical |