Metoprolol Tartrate
- Product NDC
- 60760-553
- 11-digit product format
- 607600553
- Labeler code
- 60760
- Product ID
- 60760-553_7b32e346-adbc-5a81-e053-2991aa0ab4f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2018-03-02
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 |
|---|
| 60760-553-60 | 60760055360 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-553-60) | 2018-03-02 | 0000-00-00 | No | No | Current |
| 60760-553-98 | 60760055398 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-553-98) | 2018-11-21 | 0000-00-00 | No | No | Current |