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NDC 42571-0388-30 FLUOXETINE 20 mg/1 Details
FLUOXETINE 20 mg/1
FLUOXETINE is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Micro Labs Limited. The primary component is FLUOXETINE HYDROCHLORIDE.
Product Information
| NDC | 42571-0388 |
|---|---|
| Product ID | 42571-388_0770266d-0043-f296-e063-6294a90a1d1c |
| 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 | FLUOXETINE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | FLUOXETINE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Labeler Name | Micro Labs Limited |
| Pharmaceutical Class | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA216232 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 42571-0388-30 (42571038830)
| NDC Package Code | 42571-388-30 |
|---|---|
| Billing NDC | 42571038830 |
| Package | 30 CAPSULE in 1 BOTTLE (42571-388-30) |
| Marketing Start Date | 2023-01-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |