Metoprolol Tartrate
- Product NDC
- 68071-4269
- 11-digit product format
- 680714269
- Labeler code
- 68071
- Product ID
- 68071-4269_bb78a073-9a01-6548-e053-2995a90a8fa8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2015-08-14
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- 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 |
|---|
| 68071-4269-1 | 68071426901 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-4269-1) | 2018-02-06 | 0000-00-00 | No | No | Current |