Metoprolol Tartrate
- Product NDC
- 70882-132
- 11-digit product format
- 708820132
- Labeler code
- 70882
- Product ID
- 70882-132_6478f769-c2cc-403a-ba3a-17fd73ac84c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cambridge Therapeutics Technologies, LLC
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2007-09-11
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 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 | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W5S57Y3A5L |
| Rxcui | 866514, 866924 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70882-132-60 | Metoprolol Tartrate | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70882-132 | METOPROLOL TARTRATE TABLET, FILM COATED [CAMBRIDGE THERAPEUTICS TECHNOLOGIES, LLC] | 1 | Current NDC, Legacy NDC, 1 package rows | 20171026_e3a6e812-98ef-49bd-8319-c8fb9f46be06.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 |
|---|
| 70882-132-60 | 70882013260 | 60 TABLET, FILM COATED in 1 BOTTLE (70882-132-60) | 2007-09-11 | 0000-00-00 | No | No | Current |