BACITRACIN
- Product NDC
- 42254-003
- 11-digit product format
- 422540003
- Labeler code
- 42254
- Product ID
- 42254-003_a3dc310a-3d75-4e1e-9f9f-ed5c77ff7bfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BACITRACIN
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Rebel Distributors Corp
- Application
- ANDA061212
- Marketing category
- ANDA
- Marketing start
- 2010-01-11
- Marketing end
- 0000-00-00
- Substance
- BACITRACIN
- Active strength
- 500 [iU]/g
- Pharmacologic classes
- Decreased Cell Wall Synthesis & Repair [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 42254-003-35 | BACITRACIN | 3.5 g in 1 TUBE | OINTMENT | 3.5 | | 1 |
| 42254-003-35 | BACITRACIN | 1 in 1 CARTON | OINTMENT | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42254-003 | BACITRACIN OINTMENT [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20111108_a3dc310a-3d75-4e1e-9f9f-ed5c77ff7bfe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 42254-003-35 | 42254000335 | 3.5 g in 1 TUBE | 3.5 g | Historical |