Metoprolol Tartrate
- Product NDC
- 53808-1117
- 11-digit product format
- 538081117
- Labeler code
- 53808
- Product ID
- 53808-1117_35a4a6ec-340f-4802-b4e5-bfc9af82fc46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2015-08-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53808-1117-1 | Metoprolol Tartrate | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1117 | METOPROLOL TARTRATE TABLET, FILM COATED [DOH CENTRAL PHARMACY] | 2 | Legacy NDC, 1 package rows | 20190125_ed165a1b-13c0-4093-bcaf-a3b3d7856393.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53808-1117-1 | 53808111701 | 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-1117-1) | 2015-08-14 | 0000-00-00 | No | No | Current |