ZYPREXA
- Product NDC
- 64725-7597
- 11-digit product format
- 647257597
- Labeler code
- 64725
- Product ID
- 64725-7597_5f3acc57-5fb6-4042-adf8-c2db2f41d0f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR
- Labeler
- TYA Pharmaceuticals
- Application
- NDA021253
- Marketing category
- NDA
- Marketing start
- 2004-04-01
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 10 mg/2mL
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64725-7597-1 | ZYPREXA Intramuscular | 10 mL in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-7597 | ZYPREXA INTRAMUSCULAR (OLANZAPINE) INJECTION, POWDER, FOR SOLUTION [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20160519_85688d8f-f2de-408a-8ae2-0976c266c961.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 64725-7597-1 | 64725759701 | 10 mL in 1 VIAL | 10 ml | Historical |