Metoprolol Tartrate
- Product NDC
- 0904-6342
- 11-digit product format
- 009046342
- Labeler code
- 0904
- Product ID
- 0904-6342_1d470f32-a887-4db7-9c82-a71be8ad6263
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA202871
- Marketing category
- ANDA
- Marketing start
- 2014-03-14
- 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
- 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 |
|---|
| 0904-6342-61 | 00904634261 | 100 BLISTER PACK in 1 CARTON (0904-6342-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2014-03-14 | 0000-00-00 | No | No | Current |
| 0904-6342-80 | 00904634280 | 1000 TABLET in 1 BOTTLE (0904-6342-80) | 1000 tablet | 2014-03-14 | 0000-00-00 | No | No | Current |