Metoprolol Tartrate
- Product NDC
- 0615-8017
- 11-digit product format
- 006158017
- Labeler code
- 0615
- Product ID
- 0615-8017_e51b3b3f-5a8f-4dec-a83a-dda54bc8db24
- 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
- 1993-12-23
- Marketing end
- 2023-11-30
- Substance
- METOPROLOL TARTRATE
- Active strength
- 100 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 |
|---|
| 0615-8017-30 | 00615801730 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8017-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2016-05-12 | 0000-00-00 | No | No | Current |
| 0615-8017-39 | 00615801739 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8017-39) | | 2016-05-10 | 0000-00-00 | No | No | Current |