Buspirone Hydrochloride
- Product NDC
- 60760-548
- 11-digit product format
- 607600548
- Labeler code
- 60760
- Product ID
- 60760-548_f06f040b-df21-7087-e053-2995a90ac1e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202557
- Marketing category
- ANDA
- Marketing start
- 2019-10-15
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-548-60 | 60760054860 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-548-60) | 60 tablet | 2019-10-15 | 0000-00-00 | No | No | Current |