Metoprolol Tartrate
- Product NDC
- 51655-271
- 11-digit product format
- 516550271
- Labeler code
- 51655
- Product ID
- 51655-271_d4790a90-4369-bd13-e053-2a95a90a4eb5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-271 | METOPROLOL TARTRATE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS] | 2 | Legacy NDC | 20220101_addbf0fb-c2a3-0c47-e053-2a95a90a98d8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-271-26 | 51655027126 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-271-26) | 2020-05-01 | 0000-00-00 | No | No | Current |