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NDC 27241-0252-01 Fluphenazine hydrochloride 10 mg/1 Details
Fluphenazine hydrochloride 10 mg/1
Fluphenazine hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ajanta Pharma USA Inc.. The primary component is FLUPHENAZINE HYDROCHLORIDE.
Product Information
| NDC | 27241-0252 |
|---|---|
| Product ID | 27241-252_5bfb3960-acc0-4dbf-aaa3-cdb10d4d6522 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Fluphenazine hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Fluphenazine hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
| Labeler Name | Ajanta Pharma USA Inc. |
| Pharmaceutical Class | Phenothiazine [EPC], Phenothiazines [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA217410 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 27241-0252-01 (27241025201)
| NDC Package Code | 27241-252-01 |
|---|---|
| Billing NDC | 27241025201 |
| Package | 100 TABLET in 1 BOTTLE (27241-252-01) |
| Marketing Start Date | 2023-01-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |