Bupropion hydrochloride 300 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release
Comprehensive product details for sourcing and verification.
| NDC 11 | 69097-0072-12 |
|---|---|
| Product NDC | 69097-0072 |
| Generic Drug Name | Bupropion hydrochloride |
| Brand Name | Bupropion Hydrochloride |
| Manufacturer | Cipla USA., Inc. |
| Strength | 300 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 500 Tablet, Film Coated, Extended Release |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-072-12) |
| Active Ingredients | Bupropion Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
Bupropion hydrochloride 300 mg / 1 Tablet is tracked under NDC 69097-0072-12 and rolls up into product family 69097-0072. Use this page to confirm the exact presentation before moving into related family or manufacturer pathways.
- Package configuration: 500 Tablet, Film Coated, Extended Release.
- Manufacturer: Cipla USA., Inc..
- Dosage form: Tablet.
- Family size: 1 active presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Bupropion hydrochloride 300 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release, NDC 69097-0072-12, is a Cipla USA., Inc. 300 mg / 1 tablet presentation packaged as 500 Tablet, Film Coated, Extended Release.
NDC search formats
- Canonical NDC 11: 69097-0072-12.
- Digits-only NDC 11: 69097007212.
- Possible 10-digit display format: 69097-072-12 (6909707212).
Helpful product links
- Search by brand name: Bupropion Hydrochloride.
- Exact NDC 11: 69097-0072-12.
- Product family NDC: 69097-0072.