Metoprolol Tartrate
- Product NDC
- 68788-7200
- 11-digit product format
- 687887200
- Labeler code
- 68788
- Product ID
- 68788-7200_8f2a28b3-30e5-4c09-8c82-a5e9100cf0e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2018-07-19
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE
- Active strength
- 100 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 |
|---|
| 68788-7200-1 | 68788720001 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7200-1) | 2018-07-19 | 0000-00-00 | No | No | Current |
| 68788-7200-3 | 68788720003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7200-3) | 2018-07-19 | 0000-00-00 | No | No | Current |
| 68788-7200-6 | 68788720006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7200-6) | 2018-07-19 | 0000-00-00 | No | No | Current |
| 68788-7200-9 | 68788720009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7200-9) | 2018-07-19 | 0000-00-00 | No | No | Current |