NDC 70954-159 – Clorazepate Dipotassium
Clorazepate Dipotassium 3.75 mg/1 · Tablet · Oral
Product NDC70954-159
Product details
- Brand name
- Clorazepate Dipotassium
- Generic name
- Clorazepate Dipotassium
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA213730
- Marketed since
- June 16, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Benzodiazepine
Active ingredients
- Clorazepate Dipotassium 3.75 mg/1
Uses, dosage, side effects and warnings for Clorazepate Dipotassium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70954-159-10 | 100 TABLET in 1 BOTTLE (70954-159-10) | Jun 16, 2022 |
| 70954-159-20 | 500 TABLET in 1 BOTTLE (70954-159-20) | Jul 1, 2022 |
| 70954-159-30 | 30 TABLET in 1 BOTTLE (70954-159-30) | Aug 21, 2023 |
| 70954-159-50 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (70954-159-50) / 1 TABLET in 1 BLISTER PACK (70954-159-40) | Jun 15, 2025 |
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- 60505-4755 Clorazepate Dipotassium 7.5 mg/mg · Tablet · Apotex Corp.
- 60505-4754 Clorazepate Dipotassium 3.75 mg/mg · Tablet · Apotex Corp.
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- 13107-319 Clorazepate Dipotassium 3.75 mg/1 · Tablet · Aurolife Pharma LLC
- 13107-320 Clorazepate Dipotassium 7.5 mg/1 · Tablet · Aurolife Pharma LLC
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