Prochlorperazine 00713-0135
Product NDC
00713-0135- Manufacturer
- Cosette Pharmaceuticals, Inc.
- Dosage Form
- Suppository
- Route
- Rectal
- Product Type
- Human Prescription Drug
- Marketing Start
- November 30, 1993
- Listing Expires
- December 31, 2026
- Application
- ANDA040058
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prochlorperazine | 25 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(2)
1000 BLISTER PACK in 1 CARTON (0713-0135-10) / 1 SUPPOSITORY in 1 BLISTER PACK
12 BLISTER PACK in 1 CARTON (0713-0135-12) / 1 SUPPOSITORY in 1 BLISTER PACK