Metoprolol succinate
- Product NDC
- 55700-232
- 11-digit product format
- 557000232
- Labeler code
- 55700
- Product ID
- 55700-232_65faf348-3431-412b-97cc-b4068cafcf20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA078889
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- 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
- 2023-12-31
- 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 |
|---|
| 55700-232-30 | 55700023230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-232-30) | 2015-03-20 | 0000-00-00 | No | No | Current |
| 55700-232-90 | 55700023290 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-232-90) | 2015-03-20 | 0000-00-00 | No | No | Current |