Metoprolol tartrate
- Product NDC
- 70518-3475
- 11-digit product format
- 705183475
- Labeler code
- 70518
- Product ID
- 70518-3475_e60c7ea6-4aa3-13dd-e053-2a95a90aebb2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076670
- Marketing category
- ANDA
- Marketing start
- 2022-08-11
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 70518-3475 | METOPROLOL TARTRATE TABLET [REMEDYREPACK INC.] | 3 | Legacy NDC | 20240322_61d2f702-a546-48a7-a49f-a0817020bf50.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3475-0 | 70518347500 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-3475-0) | 180 tablet | 2022-08-11 | 0000-00-00 | No | No | Current |