Metoprolol Tartrate
- Product NDC
- 59651-760
- 11-digit product format
- 596510760
- Labeler code
- 59651
- Product ID
- 59651-760_2d3b41ae-f657-4459-bdee-e76e644ec167
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2023-12-07
- Substance
- METOPROLOL TARTRATE
- Active strength
- 75 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 | 75 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 1606347, 1606349 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59651-760-01 | Metoprolol Tartrate | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59651-760 | METOPROLOL TARTRATE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 3 | Current NDC, 1 package rows | 20240224_ac4ac150-d3e6-4bd1-8a4a-7d63fade3e49.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 59651-760-01 | 59651076001 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-760-01) | 2023-12-07 | No | No | Current |