Metoprolol tartrate
- Product NDC
- 70934-186
- 11-digit product format
- 709340186
- Labeler code
- 70934
- Product ID
- 70934-186_b96b0433-4a37-726c-e053-2a95a90a9dba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA074644
- Marketing category
- ANDA
- Marketing start
- 2018-10-23
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-186-60 | 70934018660 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-186-60) | 60 tablet | 2018-10-23 | 0000-00-00 | No | No | Current |