Bupropion HCL
- Product NDC
- 72189-457
- 11-digit product format
- 721890457
- Labeler code
- 72189
- Product ID
- 72189-457_2c4dd247-ae5a-fe93-e063-6394a90a937c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion HCL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA076143
- Marketing category
- ANDA
- Marketing start
- 2023-03-30
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bupropion HCL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUPROPION HYDROCHLORIDE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZG7E5POY8O |
| Rxcui | 993687 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-457-30 | Bupropion HCL | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-457 | BUPROPION HCL TABLET, FILM COATED [DIRECT_RX] | 2 | Current NDC, 1 package rows | 20250123_f820ad7d-3c88-4a4f-e053-6294a90aef7b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-457-30 | 72189045730 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30) | 2023-03-30 | No | No | Current |