Clomipramine Hydrochloride
- Product NDC
- 70771-1012
- 11-digit product format
- 707711012
- Labeler code
- 70771
- Product ID
- 70771-1012_4264806a-a5bc-46ee-b4f6-7a1ae0dfe331
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clomipramine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA208961
- Marketing category
- ANDA
- Marketing start
- 2018-05-03
- Marketing end
- 0000-00-00
- Substance
- CLOMIPRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1012-1 | 70771101201 | 100 CAPSULE in 1 BOTTLE (70771-1012-1) | 100 capsule | 2018-05-03 | 0000-00-00 | No | No | Current |
| 70771-1012-7 | 70771101207 | 30 CAPSULE in 1 BOTTLE (70771-1012-7) | 30 capsule | 2018-05-03 | 0000-00-00 | No | No | Current |
| 70771-1012-9 | 70771101209 | 90 CAPSULE in 1 BOTTLE (70771-1012-9) | 90 capsule | 2018-05-03 | 0000-00-00 | No | No | Current |