Metoprolol succinate
- Product NDC
- 68001-121
- 11-digit product format
- 680010121
- Labeler code
- 68001
- Product ID
- 68001-121_98f8056c-5885-e243-e053-2995a90a68d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA090617
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-121-00 | 68001012100 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-121-00) | 2014-01-01 | 0000-00-00 | No | No | Current |
| 68001-121-03 | 68001012103 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-121-03) | 2014-01-01 | 0000-00-00 | No | No | Current |