Olanzapine
- Product NDC
- 70518-1535
- 11-digit product format
- 705181535
- Labeler code
- 70518
- Product ID
- 70518-1535_e530c814-4f02-7eb7-e053-2995a90a059f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076255
- Marketing category
- ANDA
- Marketing start
- 2018-10-15
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1535-0 | 70518153500 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1535-0) | 2018-10-15 | 0000-00-00 | No | No | Current |