Metoprolol Tartrate
- Product NDC
- 55289-093
- 11-digit product format
- 552890093
- Labeler code
- 55289
- Product ID
- 55289-093_adb868f9-bd13-1215-e053-2a95a90a34ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA074217
- Marketing category
- ANDA
- Marketing start
- 1994-05-27
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-093-30 | 55289009330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-093-30) | 2015-10-27 | 0000-00-00 | No | No | Current |
| 55289-093-60 | 55289009360 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-093-60) | 2015-10-27 | 0000-00-00 | No | No | Current |
| 55289-093-90 | 55289009390 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-093-90) | 2015-10-27 | 0000-00-00 | No | No | Current |
| 55289-093-93 | 55289009393 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-093-93) | 2015-10-27 | 0000-00-00 | No | No | Current |