Metoprolol Tartrate
- Product NDC
- 51079-801
- 11-digit product format
- 510790801
- Labeler code
- 51079
- Product ID
- 51079-801_3a873e83-88a2-9ea1-e063-6394a90a98c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA076704
- Marketing category
- ANDA
- Marketing start
- 1994-05-03
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metoprolol Tartrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL TARTRATE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 866514, 866924 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51079-801-01 | Metoprolol Tartrate | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 15 |
| 51079-801-20 | Metoprolol Tartrate | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 15 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| METOPROLOL TARTRATE | ACTIVE INGREDIENT | W5S57Y3A5L | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| METOPROLOL | ACTIVE MOIETY | GEB06NHM23 | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| AMMONIUM LAURETH-5 SULFATE | INACTIVE INGREDIENT | 43ZIH89I48 | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| D&C RED NO. 27 | INACTIVE INGREDIENT | 2LRS185U6K | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| POLYDEXTROSE | INACTIVE INGREDIENT | VH2XOU12IE | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | METOPROLOL TARTRATE TABLET, FILM COATED [CARDINAL HEALTH] | 9 | |
| METOPROLOL TARTRATE | ACTIVE INGREDIENT | W5S57Y3A5L | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| METOPROLOL | ACTIVE MOIETY | GEB06NHM23 | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| D&C RED NO. 27 | INACTIVE INGREDIENT | 2LRS185U6K | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| POLYDEXTROSE | INACTIVE INGREDIENT | VH2XOU12IE | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51079-801 | METOPROLOL TARTRATE TABLET, FILM COATED [MYLAN INSTITUTIONAL INC.] | 13 | Current NDC, Legacy NDC, 2 package rows | 20250115_961248d5-d53c-408d-8f8f-d31885054f96.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-801-01 | 51079080101 | 1 in 1 BLISTER PACK | | | | | | Historical |
| 51079-801-20 | 51079080120 | 100 BLISTER PACK in 1 CARTON (51079-801-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-801-01) | 100 blister pack | 1994-05-03 | 0000-00-00 | No | No | Current |