Metoprolol Tartrate
- Product NDC
- 42708-147
- 11-digit product format
- 427080147
- Labeler code
- 42708
- Product ID
- 42708-147_4586b1ca-b20b-f78a-e063-6394a90a2523
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- QPharma, Inc.
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2007-09-11
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Metoprolol Tartrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METOPROLOL TARTRATE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 866514 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42708-147-60 | Metoprolol Tartrate | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42708-147 | METOPROLOL TARTRATE TABLET, FILM COATED [QPHARMA, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250522_c0e147a8-36a6-1e61-e053-2a95a90afd62.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42708-147-60 | 42708014760 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-147-60) | 2021-04-23 | 0000-00-00 | Yes | No | Current |