Metoprolol Tartrate
- Product NDC
- 49999-575
- 11-digit product format
- 499990575
- Labeler code
- 49999
- Product ID
- 49999-575_65d3db02-1108-4c72-99c9-cdb1b7414229
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076670
- Marketing category
- ANDA
- Marketing start
- 2004-01-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49999-575-90 | 49999057590 | 90 TABLET in 1 BOTTLE (49999-575-90) | 90 tablet | 2004-01-15 | 0000-00-00 | No | No | Current |