metoprolol succinate
- Product NDC
- 70518-3122
- 11-digit product format
- 705183122
- Labeler code
- 70518
- Product ID
- 70518-3122_c4d3e9bb-695a-19d8-e053-2a95a90a9086
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203894
- Marketing category
- ANDA
- Marketing start
- 2021-06-15
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- metoprolol succinate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL SUCCINATE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TH25PD4CCB |
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3122-0 | 70518312200 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3122-0) | 2021-06-15 | 0000-00-00 | No | No | Current |