Dutasteride
- Product NDC
- 70771-1347
- 11-digit product format
- 707711347
- Labeler code
- 70771
- Product ID
- 70771-1347_a00cd4b7-4f64-4228-a425-995dcf1bc38d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dutasteride
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA204373
- Marketing category
- ANDA
- Marketing start
- 2018-05-16
- Marketing end
- 0000-00-00
- Substance
- DUTASTERIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
- 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 |
|---|
| 70771-1347 | DUTASTERIDE CAPSULE, LIQUID FILLED [ZYDUS LIFESCIENCES LIMITED] | 6 | Legacy NDC | 20241113_b8a00cff-6912-4544-8290-8c912ab2573a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1347-3 | 70771134703 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (70771-1347-3) | 2018-05-16 | 0000-00-00 | No | No | Current |
| 70771-1347-9 | 70771134709 | 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (70771-1347-9) | 2018-05-16 | 0000-00-00 | No | No | Current |