Metoprolol Tartrate
- Product NDC
- 0615-8322
- 11-digit product format
- 006158322
- Labeler code
- 0615
- Product ID
- 0615-8322_49d5fda0-a48a-41a2-9c4b-59b0521e5216
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA076704
- Marketing category
- ANDA
- Marketing start
- 2004-02-23
- Marketing end
- 2023-10-31
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8322-05 | 00615832205 | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8322-05) | | 2019-12-09 | 2023-10-31 | No | No | Current |
| 0615-8322-30 | 00615832230 | 6 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (0615-8322-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2019-12-09 | 2023-10-31 | No | No | Current |
| 0615-8322-39 | 00615832239 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8322-39) | | 2019-12-09 | 2023-10-31 | No | No | Current |