Metoprolol succinate
- Product NDC
- 68071-1921
- 11-digit product format
- 680711921
- Labeler code
- 68071
- Product ID
- 68071-1921_bc04a834-98b4-71bb-e053-2a95a90a374d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 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 |
|---|
| 68071-1921-3 | 68071192103 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-1921-3) | 2016-12-27 | 0000-00-00 | No | No | Current |
| 68071-1921-6 | 68071192106 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-1921-6) | 2016-12-27 | 0000-00-00 | No | No | Current |
| 68071-1921-9 | 68071192109 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-1921-9) | 2016-12-27 | 0000-00-00 | No | No | Current |