Bupropion Hydrochloride
- Product NDC
- 24689-120
- 11-digit product format
- 246890120
- Labeler code
- 24689
- Product ID
- 24689-120_120b51f0-f2d3-1de1-e063-6294a90a3691
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apnar Pharma LP
- Application
- ANDA075584
- Marketing category
- ANDA
- Marketing start
- 2021-12-20
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24689-120-01 | Bupropion Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24689-120 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [APNAR PHARMA LP] | 6 | Current NDC, Legacy NDC, 1 package rows | 20240224_d1830cfd-e7f4-345c-e053-2995a90a2251.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24689-120-01 | 24689012001 | 100 TABLET, FILM COATED in 1 BOTTLE (24689-120-01) | 2021-12-20 | 0000-00-00 | No | No | Current |