Metoprolol succinate
- Product NDC
- 55700-192
- 11-digit product format
- 557000192
- Labeler code
- 55700
- Product ID
- 55700-192_3b3edb95-fb8e-4a45-8b2b-b96aa6234889
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA090617
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-192-30 | 55700019230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-192-30) | 2014-12-12 | 0000-00-00 | No | No | Current |
| 55700-192-60 | 55700019260 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-192-60) | 2014-12-12 | 0000-00-00 | No | No | Current |
| 55700-192-90 | 55700019290 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-192-90) | 2014-12-12 | 0000-00-00 | No | No | Current |