Bupropion Hydrochloride 200 mg / 1 Tablet 60 Tablet, Film Coated, Extended Release
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 00115-5445-13 |
|---|---|
| Product NDC | 00115-5445 |
| Generic Drug Name | Bupropion Hydrochloride |
| Brand Name | Bupropion Hydrochloride |
| Manufacturer | Amneal Pharmaceuticals of New York LLC |
| Strength | 200 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 60 Tablet, Film Coated, Extended Release |
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-5445-13) |
| Active Ingredients | Bupropion Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
Bupropion Hydrochloride 200 mg / 1 Tablet is tracked under NDC 00115-5445-13 and rolls up into product family 00115-5445. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 60 Tablet, Film Coated, Extended Release.
- Manufacturer: Amneal Pharmaceuticals of New York LLC.
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
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Bupropion Hydrochloride 200 mg / 1 Tablet 60 Tablet, Film Coated, Extended Release, NDC 00115-5445-13, is a Amneal Pharmaceuticals of New York LLC 200 mg / 1 tablet presentation packaged as 60 Tablet, Film Coated, Extended Release.
NDC search formats
- Canonical NDC 11: 00115-5445-13
- Digits-only NDC 11: 00115544513
- Possible 10-digit display format: 0115-5445-13 (0115544513)
Helpful product links
- Search by brand name: Bupropion Hydrochloride
- NDC 11: 00115-5445-13
- Product family NDC: 00115-5445