Metoprolol Tartrate
- Product NDC
- 51655-536
- 11-digit product format
- 516550536
- Labeler code
- 51655
- Product ID
- 51655-536_1eed2ae0-5b11-49ba-abe3-9835516738f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals, LLC
- Application
- ANDA074644
- Marketing category
- ANDA
- Marketing start
- 2014-09-19
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-536 | METOPROLOL TARTRATE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 2 | Legacy NDC | 20150401_c5d7f565-6cbe-4306-b3dd-a93ab3eac094.zip |