Metoprolol Succinate
- Product NDC
- 60429-140
- 11-digit product format
- 604290140
- Labeler code
- 60429
- Product ID
- 60429-140_956e4504-c556-6cb9-e053-2995a90a58c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA076862
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- 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 |
|---|
| 60429-140-01 | 60429014001 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-140-01) | 2013-03-22 | 0000-00-00 | No | No | Current |
| 60429-140-10 | 60429014010 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-140-10) | 2013-03-22 | 0000-00-00 | No | No | Current |