Metoprolol Tartrate
- Product NDC
- 72888-197
- 11-digit product format
- 728880197
- Labeler code
- 72888
- Product ID
- 72888-197_4984fefe-6924-2aa6-e063-6394a90a1853
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METOPROLOL TARTRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advagen Pharma Limited
- Application
- NDA218698
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2025-08-28
- Substance
- METOPROLOL TARTRATE
- Active strength
- 12.5 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metoprolol Tartrate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL TARTRATE | 12.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 2723025 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72888-197-00 | Metoprolol Tartrate | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
| 72888-197-03 | Metoprolol Tartrate | 60 in 1 BOTTLE | TABLET | 60 | | 2 |
| 72888-197-30 | Metoprolol Tartrate | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72888-197-00 | 72888019700 | 1000 TABLET in 1 BOTTLE (72888-197-00) | 1000 tablet | 2025-08-28 | No | No | Historical |
| 72888-197-03 | 72888019703 | 60 TABLET in 1 BOTTLE (72888-197-03) | 60 tablet | 2026-01-25 | No | No | Historical |
| 72888-197-30 | 72888019730 | 30 TABLET in 1 BOTTLE (72888-197-30) | 30 tablet | 2025-08-28 | No | No | Historical |