Metoprolol Tartrate
- Product NDC
- 55154-6895
- 11-digit product format
- 551546895
- Labeler code
- 55154
- Product ID
- 55154-6895_8561a213-7a8f-437e-8093-270724855234
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA202871
- Marketing category
- ANDA
- Marketing start
- 2013-08-25
- Marketing end
- 2021-05-31
- 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
- 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 |
|---|
| 55154-6895-0 | 55154689500 | 10 BLISTER PACK in 1 BAG (55154-6895-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2013-08-25 | 2021-05-31 | No | No | Current |