Metoprolol Tartrate and Hydrochlorothiazide
- Product NDC
- 63629-7332
- 11-digit product format
- 636297332
- Labeler code
- 63629
- Product ID
- 63629-7332_a87f29aa-25c9-4964-84c1-2884b52b79a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202870
- Marketing category
- ANDA
- Marketing start
- 2015-10-15
- Marketing end
- 0000-00-00
- Substance
- METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE
- Active strength
- 100 mg/1; mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7332-1 | 63629733201 | 30 TABLET in 1 BOTTLE (63629-7332-1) | 30 tablet | 2017-07-18 | 0000-00-00 | No | No | Current |
| 63629-7332-2 | 63629733202 | 8 TABLET in 1 BOTTLE (63629-7332-2) | 8 tablet | 2017-07-18 | 0000-00-00 | No | No | Current |