Metoprolol Succinate
- Product NDC
- 71335-0523
- 11-digit product format
- 713350523
- Labeler code
- 71335
- Product ID
- 71335-0523_f3be5b47-00ca-47c4-960e-0c34c49b6fec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076862
- Marketing category
- ANDA
- Marketing start
- 2009-08-04
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-0523-1 | 71335052301 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0523-1) | 2010-05-12 | 0000-00-00 | No | No | Current |
| 71335-0523-2 | 71335052302 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0523-2) | 2010-05-12 | 0000-00-00 | No | No | Current |
| 71335-0523-3 | 71335052303 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0523-3) | 2010-05-12 | 0000-00-00 | No | No | Current |
| 71335-0523-4 | 71335052304 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0523-4) | 2010-05-12 | 0000-00-00 | No | No | Current |
| 71335-0523-5 | 71335052305 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0523-5) | 2010-05-12 | 0000-00-00 | No | No | Current |