metoprolol succinate
- Product NDC
- 16714-855
- 11-digit product format
- 167140855
- Labeler code
- 16714
- Product ID
- 16714-855_aa40c17c-d04a-4e23-aaab-6283cb37ee24
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA203894
- Marketing category
- ANDA
- Marketing start
- 2018-08-27
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 200 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 |
|---|
| 16714-855 | METOPROLOL SUCCINATE TABLET, EXTENDED RELEASE [NORTHSTAR RX LLC] | 10 | Legacy NDC | 20240915_c11994cf-e88b-4cbe-a2b0-c06eae3a09aa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-855-01 | 16714085501 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-855-01) | 2018-08-27 | 0000-00-00 | No | No | Current |
| 16714-855-02 | 16714085502 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-855-02) | 2018-08-27 | 0000-00-00 | No | No | Current |