Metoprolol Succinate
- Product NDC
- 64679-849
- 11-digit product format
- 646790849
- Labeler code
- 64679
- Product ID
- 64679-849_d2adade1-b010-fdf2-e053-2995a90a6bd5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA203699
- Marketing category
- ANDA
- Marketing start
- 2021-02-26
- 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
- 2022-12-31
- 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 |
|---|
| 64679-849-02 | 64679084902 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-849-02) | 2021-02-26 | 0000-00-00 | No | No | Current |
| 64679-849-03 | 64679084903 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-849-03) | 2021-02-26 | 0000-00-00 | No | No | Current |