Buspirone HCl
- Product NDC
- 21695-256
- 11-digit product format
- 216950256
- Labeler code
- 21695
- Product ID
- 21695-256_0eefdd8d-7745-47ae-a204-f35687f3db11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA074253
- Marketing category
- ANDA
- Marketing start
- 2001-03-28
- Marketing end
- 0000-00-00
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-256-60 | Buspirone HCl | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 21695-256-90 | Buspirone HCl | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-256 | BUSPIRONE HCL (BUSPIRONE HYDROCHLORIDE) TABLET [REBEL DISTRIBUTORS CORP.] | 1 | Legacy NDC, 2 package rows | 20100921_0eefdd8d-7745-47ae-a204-f35687f3db11.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-256-60 | 21695025660 | 60 in 1 BOTTLE | Historical |
| 21695-256-90 | 21695025690 | 90 in 1 BOTTLE | Historical |