Metoprolol Succinate
- Product NDC
- 51655-569
- 11-digit product format
- 516550569
- Labeler code
- 51655
- Product ID
- 51655-569_ca46025d-9c5b-7e8c-e053-2a95a90aed7e
- 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
- 2021-02-02
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 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 |
|---|
| 51655-569-52 | 51655056952 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-569-52) | 2021-02-02 | 0000-00-00 | No | No | Current |