Metoprolol Tartrate
- Product NDC
- 50090-7363
- 11-digit product format
- 500907363
- Labeler code
- 50090
- Product ID
- 50090-7363_c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2007-09-11
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 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 | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 866924 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7363-0 | Metoprolol Tartrate | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 21 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7363 | METOPROLOL TARTRATE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 21 | Current NDC, 1 package rows | 20241024_771c262d-e1db-4a75-9609-110c27c43e51.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7363-0 | 50090736300 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7363-0) | 2024-10-18 | No | No | Current |