NDC 51672-4042 – Clorazepate Dipotassium
Clorazepate Dipotassium 3.75 mg/1 · Tablet · Oral
Product NDC51672-4042
Product details
- Brand name
- Clorazepate Dipotassium
- Generic name
- Clorazepate Dipotassium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075731
- Marketed since
- April 27, 2000
- Listing expires
- December 31, 2027
- Pharmacologic class
- Benzodiazepine
Active ingredients
- Clorazepate Dipotassium 3.75 mg/1
Uses, dosage, side effects and warnings for Clorazepate Dipotassium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4042-1 | 100 TABLET in 1 BOTTLE (51672-4042-1) | Apr 27, 2000 |
| 51672-4042-2 | 500 TABLET in 1 BOTTLE (51672-4042-2) | Apr 27, 2000 |
| 51672-4042-3 | 1000 TABLET in 1 BOTTLE (51672-4042-3) | Apr 27, 2000 |
Other Clorazepate Dipotassium products
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- 70954-158 Clorazepate Dipotassium 7.5 mg/1 · Tablet · ANI Pharmaceuticals, Inc.
- 70954-159 Clorazepate Dipotassium 3.75 mg/1 · Tablet · ANI Pharmaceuticals, Inc.
- 60505-4756 Clorazepate Dipotassium 15 mg/mg · Tablet · Apotex Corp.
- 60505-4754 Clorazepate Dipotassium 3.75 mg/mg · Tablet · Apotex Corp.
- 60505-4755 Clorazepate Dipotassium 7.5 mg/mg · Tablet · Apotex Corp.
- 13107-282 Clorazepate Dipotassium 3.75 mg/1 · Tablet · Aurolife Pharma LLC
- 13107-283 Clorazepate Dipotassium 7.5 mg/1 · Tablet · Aurolife Pharma LLC
- 13107-284 Clorazepate Dipotassium 15 mg/1 · Tablet · Aurolife Pharma LLC
- 13107-319 Clorazepate Dipotassium 3.75 mg/1 · Tablet · Aurolife Pharma LLC
- 13107-320 Clorazepate Dipotassium 7.5 mg/1 · Tablet · Aurolife Pharma LLC
- 13107-321 Clorazepate Dipotassium 15 mg/1 · Tablet · Aurolife Pharma LLC