Metoprolol Tartrate
- Product NDC
- 60760-295
- 11-digit product format
- 607600295
- Labeler code
- 60760
- Product ID
- 60760-295_8a1d8fbb-096b-3d14-e053-2a95a90a288b
- 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
- 2019-05-17
- 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
- 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 |
|---|
| 60760-295-90 | 60760029590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-295-90) | 2019-05-17 | 0000-00-00 | No | No | Current |