Metoprolol Tartrate
- Product NDC
- 68071-4356
- 11-digit product format
- 680714356
- Labeler code
- 68071
- Product ID
- 68071-4356_bb7ba4c6-0c5e-286e-e053-2995a90ae33c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA200981
- Marketing category
- ANDA
- Marketing start
- 2015-08-14
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 68071-4356-3 | 68071435603 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4356-3) | 2018-03-26 | 0000-00-00 | No | No | Current |
| 68071-4356-6 | 68071435606 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-4356-6) | 2018-03-26 | 0000-00-00 | No | No | Current |
| 68071-4356-8 | 68071435608 | 180 TABLET, FILM COATED in 1 BOTTLE (68071-4356-8) | 2018-03-26 | 0000-00-00 | No | No | Current |
| 68071-4356-9 | 68071435609 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4356-9) | 2018-03-26 | 0000-00-00 | No | No | Current |