Prazosin Hydrochloride
- Product NDC
- 70518-2705
- 11-digit product format
- 705182705
- Labeler code
- 70518
- Product ID
- 70518-2705_e997ab1a-d236-7074-e053-2a95a90a8220
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210971
- Marketing category
- ANDA
- Marketing start
- 2020-04-23
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2705 | PRAZOSIN HYDROCHLORIDE CAPSULE [REMEDYREPACK INC.] | 10 | Legacy NDC | 20250328_18227ac0-f8c2-41a1-931c-cebba89a50a2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2705-0 | 70518270500 | 30 CAPSULE in 1 BLISTER PACK (70518-2705-0) | 30 capsule | 2020-04-23 | 0000-00-00 | No | No | Current |
| 70518-2705-1 | 70518270501 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2705-1) | 30 capsule | 2022-02-21 | 0000-00-00 | No | No | Current |
| 70518-2705-2 | 70518270502 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2705-2) | 30 capsule | 2022-09-26 | 0000-00-00 | No | No | Current |