BUSPIRONE HYDROCHLORIDE
- Product NDC
- 71335-2081
- 11-digit product format
- 713352081
- Labeler code
- 71335
- Product ID
- 71335-2081_a764c113-34fb-4f9d-837b-ac8c53488b2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUSPIRONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078246
- Marketing category
- ANDA
- Marketing start
- 2020-02-21
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BUSPIRONE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUSPIRONE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866083 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2081-1 | 71335208101 | 30 TABLET in 1 BOTTLE (71335-2081-1) | 30 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-2081-2 | 71335208102 | 60 TABLET in 1 BOTTLE (71335-2081-2) | 60 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-2081-3 | 71335208103 | 90 TABLET in 1 BOTTLE (71335-2081-3) | 90 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-2081-4 | 71335208104 | 45 TABLET in 1 BOTTLE (71335-2081-4) | 45 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-2081-5 | 71335208105 | 180 TABLET in 1 BOTTLE (71335-2081-5) | 180 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-2081-6 | 71335208106 | 120 TABLET in 1 BOTTLE (71335-2081-6) | 120 tablet | 2022-05-02 | 0000-00-00 | No | No | Current |