Metoprolol Succinate
- Product NDC
- 72789-010
- 11-digit product format
- 727890010
- Labeler code
- 72789
- Product ID
- 72789-010_4832e889-c60c-78aa-e063-6394a90acc69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA204106
- Marketing category
- ANDA
- Marketing start
- 2018-02-06
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 50 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 Succinate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL SUCCINATE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TH25PD4CCB |
| Rxcui | 866436 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-010-30 | Metoprolol Succinate | 30 in 1 BOTTLE, PLASTIC | TABLET, EXTENDED RELEASE | 30 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-010 | METOPROLOL SUCCINATE TABLET, EXTENDED RELEASE [PD-RX PHARMACEUTICALS, INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20240125_ff3eaf6a-5697-4ad9-98c4-86925e6da257.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-010-30 | 72789001030 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-010-30) | 2019-09-12 | 0000-00-00 | No | No | Current |