Ciprofloxacin
- Product NDC
- 63304-710
- 11-digit product format
- 633040710
- Labeler code
- 63304
- Product ID
- 63304-710_aa0b6a4a-f8ff-4d09-8813-2d58192c08c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ranbaxy Pharmaceuticals Inc.
- Application
- ANDA075747
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- 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 |
|---|
| 63304-710-01 | Ciprofloxacin | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 3 |
| 63304-710-05 | Ciprofloxacin | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 3 |
| 63304-710-14 | Ciprofloxacin | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 3 |
| 63304-710-80 | Ciprofloxacin | 100 in 1 BLISTER PACK | TABLET, FILM COATED | 100 | | 3 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CIPROFLOXACIN HYDROCHLORIDE | ACTIVE INGREDIENT | 4BA73M5E37 | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| CIPROFLOXACIN | ACTIVE MOIETY | 5E8K9I0O4U | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63304-710 | CIPROFLOXACIN TABLET, FILM COATED [RANBAXY PHARMACEUTICALS INC.] | 3 | Legacy NDC, 4 package rows | 20130930_563e576e-6966-4f8d-91bb-0a1a951de324.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63304-710-01 | 63304071001 | 100 in 1 BOTTLE | Historical |
| 63304-710-05 | 63304071005 | 500 in 1 BOTTLE | Historical |
| 63304-710-14 | 63304071014 | 14 in 1 BOTTLE | Historical |
| 63304-710-80 | 63304071080 | 100 in 1 BLISTER PACK | Historical |