Metoprolol Tartrate
- Product NDC
- 63629-8104
- 11-digit product format
- 636298104
- Labeler code
- 63629
- Product ID
- 63629-8104_13d5e9d6-e604-47ee-bea5-9fac5637f1ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2018-12-01
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8104-1 | 63629810401 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8104-1) | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8104-2 | 63629810402 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8104-2) | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8104-3 | 63629810403 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-8104-3) | 2019-07-25 | 0000-00-00 | No | No | Current |