Metoprolol Succinate
- Product NDC
- 51655-615
- 11-digit product format
- 516550615
- Labeler code
- 51655
- Product ID
- 51655-615_ca3b0d40-6aa2-7b09-e053-2995a90a200e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals, LLC
- Application
- ANDA207206
- Marketing category
- ANDA
- Marketing start
- 2021-02-19
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-615-26 | 51655061526 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-615-26) | 2021-02-26 | 0000-00-00 | No | No | Current |
| 51655-615-52 | 51655061552 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-615-52) | 2021-02-19 | 0000-00-00 | No | No | Current |