Olanzapine
- Product NDC
- 68071-2720
- 11-digit product format
- 680712720
- Labeler code
- 68071
- Product ID
- 68071-2720_df73d27f-b566-7612-e053-2995a90a167d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olanzapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmceuticals,Inc.
- Application
- ANDA202862
- Marketing category
- ANDA
- Marketing start
- 2014-08-22
- Marketing end
- 0000-00-00
- Substance
- OLANZAPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68071-2720-6 | Olanzapine | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2720 | OLANZAPINE TABLET, FILM COATED [NUCARE PHARMCEUTICALS,INC.] | 1 | Legacy NDC, 1 package rows | 20220521_df73e518-caea-a73b-e053-2995a90a69f5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2720-6 | 68071272006 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-2720-6) | 2022-05-20 | 0000-00-00 | No | No | Current |