Metoprolol tartrate
- Product NDC
- 70518-3503
- 11-digit product format
- 705183503
- Labeler code
- 70518
- Product ID
- 70518-3503_e78eba2f-44fa-62a6-e053-2a95a90a5baf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074644
- Marketing category
- ANDA
- Marketing start
- 2022-08-31
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 100 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3503-0 | 70518350300 | 30 TABLET in 1 BLISTER PACK (70518-3503-0) | 30 tablet | 2022-08-31 | 0000-00-00 | No | No | Current |