Buspirone Hydrochloride
- Product NDC
- 55700-869
- 11-digit product format
- 557000869
- Labeler code
- 55700
- Product ID
- 55700-869_aa37484f-ea24-4c97-9fe0-b2b920f1652c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA210907
- Marketing category
- ANDA
- Marketing start
- 2020-06-11
- 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 |
|---|
| 55700-869-60 | 55700086960 | 60 TABLET in 1 BOTTLE, PLASTIC (55700-869-60) | 60 tablet | 2020-06-11 | 0000-00-00 | No | No | Current |
| 55700-869-90 | 55700086990 | 90 TABLET in 1 BOTTLE, PLASTIC (55700-869-90) | 90 tablet | 2020-06-11 | 0000-00-00 | No | No | Current |