Bupropion Hydrochloride
- Product NDC
- 50436-3541
- 11-digit product format
- 504363541
- Labeler code
- 50436
- Product ID
- 50436-3541_47aab8c4-4f41-4e5d-aaf0-9427fe9c789c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA079095
- Marketing category
- ANDA
- Marketing start
- 2009-07-02
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 150 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
- 2020-12-31
- 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 |
|---|
| 50436-3541-1 | Bupropion HydrochlorideSR | 57 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 57 | | 2 |
| 50436-3541-2 | Bupropion HydrochlorideSR | 60 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3541 | BUPROPION HYDROCHLORIDE SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 2 | Legacy NDC, 2 package rows | 20190222_edc9d7ad-5ba2-4a3d-91a3-df9042fdc3dd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-3541-1 | 50436354101 | 57 in 1 BOTTLE | Historical |
| 50436-3541-2 | 50436354102 | 60 in 1 BOTTLE | Historical |