NDC 70954-021-30 - Prazosin Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70954-021
- Requested NDC
- 70954-021-30
- Package NDCs from labels
- 70954-021-10, 70954-021-20, 70954-021-30, 70954-021-40
- Manufacturer
- Major Pharmaceuticals
- Effective date
- 2026-09-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Prazosin Hydrochloride - Major Pharmaceuticals | Major Pharmaceuticals | 2026-09-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Prazosin Hydrochloride Capsules, USP 1 mg, 2 mg and 5 mg | ANI Pharmaceuticals, Inc. | 2026-07-10 | Human Prescription Drug Label |
| Prazosin Hydrochloride - Coupler LLC | Coupler LLC | 2026-06-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Prazosin Hydrochloride - Marlex Pharmaceuticals Inc | Marlex Pharmaceuticals Inc | 2025-11-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Prazosin Hydrochloride Capsules, USP 1 mg, 2 mg and 5 mg | Preferred Pharmaceuticals Inc. | 2025-09-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Prazosin Hydrochloride Capsules, USP 1 mg, 2 mg and 5 mg | REMEDYREPACK INC. | 2025-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Prazosin Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2021-12-23 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70954-021-10 | Prazosin Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | 7 | |
| 70954-021-20 | Prazosin Hydrochloride | 250 in 1 BOTTLE | CAPSULE | 250 | 7 | |
| 70954-021-30 | Prazosin Hydrochloride | 1 in 1 BLISTER PACK | CAPSULE | 1 | 7 | |
| 70954-021-40 | Prazosin Hydrochloride | 100 in 1 CARTON | CAPSULE | 100 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70954-021-10 | EA - Each | 70954-021 | bde01541-b2f0-418e-a56c-a2a87252a58e | 1 | 2018-11-06 |
| 70954-021-20 | EA - Each | 70954-021 | e101f420-f79d-4430-a973-0c5e670882ae | 1 | 2018-11-06 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.