Metoprolol succinate
- Product NDC
- 62732-1046
- 11-digit product format
- 627321046
- Labeler code
- 62732
- Product ID
- 62732-1046_bbaa578d-69e1-5407-e053-2995a90a5ed3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Yichang Humanwell Pharmaceutical Co., Ltd.
- Application
- ANDA213854
- Marketing category
- ANDA
- Marketing start
- 2021-12-30
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 62732-1046-1 | 62732104601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62732-1046-1) | 2021-12-30 | 0000-00-00 | No | No | Current |
| 62732-1046-2 | 62732104602 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62732-1046-2) | 2021-12-30 | 0000-00-00 | No | No | Current |
| 62732-1046-3 | 62732104603 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62732-1046-3) | 2021-12-30 | 0000-00-00 | No | No | Current |