BUSPIRONE HYDROCHLORIDE
- Product NDC
- 72189-200
- 11-digit product format
- 721890200
- Labeler code
- 72189
- Product ID
- 72189-200_4c498a8f-f65a-5df5-e063-6394a90ae0fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUSPIRONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA202330
- Marketing category
- ANDA
- Marketing start
- 2021-04-12
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866083 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-200-82 | BUSPIRONE HYDROCHLORIDE | 180 in 1 BOTTLE | TABLET | 180 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-200 | BUSPIRONE HYDROCHLORIDE TABLET [DIRECT RX] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250119_bae98d45-e192-56e3-e053-2a95a90aadc3.zip |
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 |
|---|
| 72189-200-82 | 72189020082 | 180 TABLET in 1 BOTTLE (72189-200-82) | 180 tablet | 2021-04-12 | 0000-00-00 | No | No | Current |