Metoprolol Tartrate
- Product NDC
- 70518-3606
- 11-digit product format
- 705183606
- Labeler code
- 70518
- Product ID
- 70518-3606_f202f8b0-d56d-9117-e053-2a95a90a97bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2023-01-04
- Marketing end
- 0000-00-00
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3606 | METOPROLOL TARTRATE TABLET, FILM COATED [REMEDYREPACK INC.] | 6 | Legacy NDC | 20250212_18294e2a-62ef-4b74-9649-50d957d88a1d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3606-0 | 70518360600 | 60 TABLET, FILM COATED in 1 BLISTER PACK (70518-3606-0) | 2023-01-04 | 0000-00-00 | No | No | Current |