Metoprolol Tartrate and Hydrochlorothiazide
- Product NDC
- 63629-7331
- 11-digit product format
- 636297331
- Labeler code
- 63629
- Product ID
- 63629-7331_f18b9c37-7176-44ae-87aa-6d18d20f23ab
- 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
- HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-7331-1 | 63629733101 | 30 TABLET in 1 BOTTLE (63629-7331-1) | 30 tablet | 2017-07-18 | 0000-00-00 | No | No | Current |