Metoprolol Succinate
- Product NDC
- 72789-145
- 11-digit product format
- 727890145
- Labeler code
- 72789
- Product ID
- 72789-145_e090dc7c-5758-558f-e053-2a95a90a59a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA207206
- Marketing category
- ANDA
- Marketing start
- 2019-10-01
- 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
- 2023-12-31
- 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 |
|---|
| 72789-145-30 | 72789014530 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-145-30) | 2020-11-03 | 0000-00-00 | No | No | Current |