NDC 16714-850 – Clomipramine Hydrochloride
Clomipramine Hydrochloride 50 mg/1 · Capsule · Oral
Product NDC16714-850
Product details
- Brand name
- Clomipramine Hydrochloride
- Generic name
- Clomipramine Hydrochloride
- Labeler
- Northstar Rx LLC.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA208961
- Marketed since
- August 27, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Clomipramine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Clomipramine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 16714-850-01 | 30 CAPSULE in 1 BOTTLE (16714-850-01) | Aug 27, 2018 |
| 16714-850-02 | 90 CAPSULE in 1 BOTTLE (16714-850-02) | Aug 27, 2018 |
| 16714-850-03 | 100 CAPSULE in 1 BOTTLE (16714-850-03) | Aug 27, 2018 |
Recalls mentioning this NDC
- D-0152-2026 Nov 12, 2025 · Class II
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable intake limit. - D-0153-2026 Nov 12, 2025 · Class II
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable intake limit. - D-0154-2026 Nov 12, 2025 · Class II
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable intake limit.
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