Metoprolol Tartrate
- Product NDC
- 70860-300
- 11-digit product format
- 708600300
- Labeler code
- 70860
- Product ID
- 70860-300_d02e25f4-72ce-441e-839a-aaf0c6416f34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA204205
- Marketing category
- ANDA
- Marketing start
- 2017-01-01
- Marketing end
- 2022-04-30
- Substance
- METOPROLOL TARTRATE
- Active strength
- 5 mg/5mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-300-05 | 70860030005 | 10 VIAL, SINGLE-DOSE in 1 CARTON (70860-300-05) > 5 mL in 1 VIAL, SINGLE-DOSE (70860-300-41) | 2017-01-01 | 0000-00-00 | No | No | Current |