Metoprolol Tartrate
- Product NDC
- 0409-2285
- 11-digit product format
- 004092285
- Labeler code
- 0409
- Product ID
- 0409-2285_3be4b7c6-7fa7-458a-b53a-90042e4e8e0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METOPROLOL TARTRATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA075160
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record