Buspirone Hydrochloride
- Product NDC
- 68071-3229
- 11-digit product format
- 680713229
- Labeler code
- 68071
- Product ID
- 68071-3229_bb14cd9b-672d-4a2f-e053-2a95a90a013a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3229-2 | 68071322902 | 20 TABLET in 1 BOTTLE (68071-3229-2) | 20 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3229-3 | 68071322903 | 30 TABLET in 1 BOTTLE (68071-3229-3) | 30 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3229-6 | 68071322906 | 60 TABLET in 1 BOTTLE (68071-3229-6) | 60 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3229-9 | 68071322909 | 90 TABLET in 1 BOTTLE (68071-3229-9) | 90 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |