Metoprolol Tartrate
- Product NDC
- 68788-8249
- 11-digit product format
- 687888249
- Labeler code
- 68788
- Product ID
- 68788-8249_ab742f5b-e10f-4818-b3c4-bd19985b9722
- 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
- 2022-08-19
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W5S57Y3A5L | METOPROLOL TARTRATE | 56392-17-7 | METOPROLOL TARTRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8249-1 | 68788824901 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8249-1) | 2022-08-19 | No | No | Historical |
| 68788-8249-3 | 68788824903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8249-3) | 2022-08-19 | No | No | Historical |
| 68788-8249-6 | 68788824906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8249-6) | 2022-08-19 | No | No | Historical |
| 68788-8249-9 | 68788824909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8249-9) | 2022-08-19 | No | No | Historical |