Metoprolol Tartrate
- Product NDC
- 0615-6547
- 11-digit product format
- 006156547
- Labeler code
- 0615
- Product ID
- 0615-6547_7f0a41c0-5c36-4e21-bcc3-69714d6386e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076704
- Marketing category
- ANDA
- Marketing start
- 2011-05-05
- Marketing end
- 2021-08-31
- 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 |
|---|
| 0615-6547-05 | 00615654705 | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-6547-05) | | 2013-01-08 | 2021-07-31 | No | No | Current |
| 0615-6547-30 | 00615654730 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-6547-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2014-09-19 | 2021-08-31 | No | No | Current |
| 0615-6547-39 | 00615654739 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6547-39) | | 2013-01-08 | 2021-08-31 | No | No | Current |