Metoprolol Tartrate
- Product NDC
- 84549-778
- 11-digit product format
- 845490778
- Labeler code
- 84549
- Product ID
- 84549-778_3ef0affa-a2fa-92de-e063-6294a90ad4d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METOPROLOL TARTRATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- ANDA078085
- Marketing category
- ANDA
- Marketing start
- 2008-07-24
- Substance
- METOPROLOL TARTRATE
- Active strength
- 1 mg/mL
- 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 | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 866508 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-778-05 | Metoprolol Tartrate | 5 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 5 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-778-05 | 84549077805 | 5 mL in 1 VIAL, SINGLE-DOSE (84549-778-05) | 5 ml | 2025-09-16 | No | No | Current |