ZYPREXA
- Product NDC
- 0002-7636
- 11-digit product format
- 000027636
- Labeler code
- 0002
- Product ID
- 0002-7636_0a5b6cfe-5486-4622-a362-f1afd9bd8f56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine pamoate
- Dosage form
- KIT
- Route
- INTRAMUSCULAR
- Labeler
- Eli Lilly and Company
- Application
- NDA022173
- Marketing category
- NDA
- Marketing start
- 2009-12-11
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0002-7636 | ZYPREXA RELPREVV (OLANZAPINE PAMOATE) KIT [ELI LILLY AND COMPANY] | 64 | Legacy NDC | 20250110_f9a73185-88de-4d7b-b3c0-bbf231483241.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0002-7636-11 | 00002763611 | 1 KIT in 1 CARTON (0002-7636-11) * 2 mL in 1 VIAL (0002-7659-01) * 3 mL in 1 VIAL (0002-7622-01) | 1 kit | 2010-03-01 | 0000-00-00 | No | No | Current |