Doxazosin
- Product NDC
- 70518-0839
- 11-digit product format
- 705180839
- Labeler code
- 70518
- Product ID
- 70518-0839_a58e0835-66d9-1a65-e053-2995a90a20ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin Mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075536
- Marketing category
- ANDA
- Marketing start
- 2017-11-10
- Marketing end
- 0000-00-00
- Substance
- DOXAZOSIN MESYLATE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],alpha-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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0839-1 | 70518083901 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0839-1) | 90 tablet | 2018-12-31 | 0000-00-00 | No | No | Current |