Metoprolol Tartrate
- Product NDC
- 71335-0996
- 11-digit product format
- 713350996
- Labeler code
- 71335
- Product ID
- 71335-0996_33a88c4b-9b51-4bef-a5ba-d09481e7ae9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074217
- Marketing category
- ANDA
- Marketing start
- 1994-05-27
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0996-1 | 71335099601 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0996-1) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 71335-0996-2 | 71335099602 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0996-2) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 71335-0996-3 | 71335099603 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0996-3) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 71335-0996-4 | 71335099604 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0996-4) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 71335-0996-5 | 71335099605 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0996-5) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 71335-0996-6 | 71335099606 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0996-6) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 71335-0996-7 | 71335099607 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0996-7) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 71335-0996-8 | 71335099608 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0996-8) | 2013-10-08 | 0000-00-00 | No | No | Current |