Trientine hydrochloride
- Product NDC
- 70710-1203
- 11-digit product format
- 707101203
- Labeler code
- 70710
- Product ID
- 70710-1203_5595b9a4-aa3e-4151-9bd5-32dd502b0b79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trientine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA211554
- Marketing category
- ANDA
- Marketing start
- 2019-04-29
- Marketing end
- 0000-00-00
- Substance
- TRIENTINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Metal Chelating Activity [MoA], Metal Chelator [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 |
|---|
| 70710-1203 | TRIENTINE HYDROCHLORIDE CAPSULE [ZYDUS PHARMACEUTICALS USA INC.] | 2 | Legacy NDC | 20221115_98548636-c8bc-449b-9494-86abac9f2edc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70710-1203-1 | 70710120301 | 1 BOTTLE in 1 CARTON (70710-1203-1) > 100 CAPSULE in 1 BOTTLE | 1 bottle | 2019-04-29 | 0000-00-00 | No | No | Current |