Metoprolol succinate
- Product NDC
- 53002-1612
- 11-digit product format
- 530021612
- Labeler code
- 53002
- Product ID
- 53002-1612_d652ef3a-2657-416d-bc8a-c51f800a2601
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA090617
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53002-1612-0 | Metoprolol succinate | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 3 |
| 53002-1612-3 | Metoprolol succinate | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-1612 | METOPROLOL SUCCINATE TABLET, EXTENDED RELEASE [RPK PHARMACEUTICALS, INC.] | 3 | Legacy NDC, 2 package rows | 20230609_295516b3-19e4-42e6-ae81-b7e1e8750041.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 |
|---|
| 53002-1612-0 | 53002161200 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-1612-0) | 2019-06-01 | 0000-00-00 | No | No | Current |
| 53002-1612-3 | 53002161203 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-1612-3) | 2019-06-01 | 0000-00-00 | No | No | Current |