Terazosin
- Product NDC
- 70518-0342
- 11-digit product format
- 705180342
- Labeler code
- 70518
- Product ID
- 70518-0342_522d3d90-4456-513c-e063-6394a90a1046
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Terazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075317
- Marketing category
- ANDA
- Marketing start
- 2017-03-20
- Substance
- TERAZOSIN HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Terazosin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TERAZOSIN HYDROCHLORIDE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | D32S14F082 |
| Rxcui | 313215 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-0342-0 | Terazosin | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0342 | TERAZOSIN (TERAZOSIN HYDROCHLORIDE) CAPSULE [REMEDYREPACK INC.] | 9 | Current NDC, Legacy NDC, 1 package rows | 20250426_242589f0-0c79-4ea1-b900-10bccfec2b82.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0342-0 | 70518034200 | 30 CAPSULE in 1 BLISTER PACK (70518-0342-0) | 30 capsule | 2017-03-20 | 0000-00-00 | No | No | Current |