Metoprolol Succinate
- Product NDC
- 60429-142
- 11-digit product format
- 604290142
- Labeler code
- 60429
- Product ID
- 60429-142_b1aaf915-f539-4e8a-e053-2995a90ab380
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA077298
- Marketing category
- ANDA
- Marketing start
- 2010-04-15
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 60429-142-01 | 60429014201 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-142-01) | 2010-04-15 | 0000-00-00 | No | No | Current |
| 60429-142-10 | 60429014210 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-142-10) | 2010-04-15 | 0000-00-00 | No | No | Current |