Metoprolol Tartrate
- Product NDC
- 60760-243
- 11-digit product format
- 607600243
- Labeler code
- 60760
- Product ID
- 60760-243_985a1aef-61bb-14fc-e053-2a95a90ab21f
- 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
- 2019-08-12
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-243 | METOPROLOL TARTRATE (METOPROLOL TARTRATE) TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] | 3 | Legacy NDC | 20250110_903cdf86-c31c-1d65-e053-2995a90ac6b7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-243-60 | 60760024360 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-243-60) | 2019-08-12 | 0000-00-00 | No | No | Current |
| 60760-243-98 | 60760024398 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-243-98) | 2019-11-21 | 0000-00-00 | No | No | Current |