Buspirone Hydrochloride
- Product NDC
- 70518-0682
- 11-digit product format
- 705180682
- Labeler code
- 70518
- Product ID
- 70518-0682_47fb4ce6-787a-6467-e063-6294a90ace55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2017-08-16
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Buspirone Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUSPIRONE HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866094 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-0682-0 | Buspirone Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 13 |
| 70518-0682-1 | Buspirone Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 13 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0682-0 | 70518068200 | 30 TABLET in 1 BLISTER PACK (70518-0682-0) | 30 tablet | 2017-08-16 | | No | No | Historical |
| 70518-0682-1 | 70518068201 | 30 TABLET in 1 BLISTER PACK (70518-0682-1) | 30 tablet | 2021-01-20 | 0000-00-00 | No | No | Current |