Metoprolol Tartrate
- Product NDC
- 71205-701
- 11-digit product format
- 712050701
- Labeler code
- 71205
- Product ID
- 71205-701_f8f39b5f-846f-48f1-b5b0-e6e5c7302bda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2018-12-01
- Substance
- METOPROLOL TARTRATE
- Active strength
- 50 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 |
|---|
| 71205-701-30 | 71205070130 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-701-30) | 2022-09-21 | No | No | Historical |
| 71205-701-60 | 71205070160 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-701-60) | 2022-09-21 | No | No | Historical |
| 71205-701-90 | 71205070190 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-701-90) | 2022-09-21 | No | No | Historical |