Metoprolol Tartrate
- Product NDC
- 68071-1795
- 11-digit product format
- 680711795
- Labeler code
- 68071
- Product ID
- 68071-1795_bb18e6d8-d995-60ca-e053-2a95a90ab663
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077739
- Marketing category
- ANDA
- Marketing start
- 2007-09-11
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1795-1 | 68071179501 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-1795-1) | 2017-07-17 | 0000-00-00 | No | No | Current |