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NDC 70518-0921-00 Olanzapine 10 mg/1 Details
Olanzapine 10 mg/1
Olanzapine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is OLANZAPINE.
Product Information
NDC | 70518-0921 |
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Product ID | 70518-0921_f54ea036-a44e-cfda-e053-2995a90aa3a3 |
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 | Olanzapine |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Olanzapine |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 10 |
Active Ingredient Units | mg/1 |
Substance Name | OLANZAPINE |
Labeler Name | REMEDYREPACK INC. |
Pharmaceutical Class | Atypical Antipsychotic [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA202862 |
Listing Certified Through | 2024-12-31 |
Package
NDC 70518-0921-00 (70518092100)
NDC Package Code | 70518-0921-0 |
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Billing NDC | 70518092100 |
Package | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0921-0) |
Marketing Start Date | 2017-12-26 |
NDC Exclude Flag | N |
Pricing Information | N/A |