Metoprolol succinate
- Product NDC
- 68071-2191
- 11-digit product format
- 680712191
- Labeler code
- 68071
- Product ID
- 68071-2191_bc091f58-6263-5757-e053-2a95a90ac460
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA090617
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 25 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 |
|---|
| 68071-2191-3 | 68071219103 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2191-3) | 2017-03-28 | 0000-00-00 | No | No | Current |
| 68071-2191-6 | 68071219106 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2191-6) | 2017-03-28 | 0000-00-00 | No | No | Current |
| 68071-2191-9 | 68071219109 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2191-9) | 2017-03-28 | 0000-00-00 | No | No | Current |