Ranitidine
- Product NDC
- 60505-2880
- 11-digit product format
- 605052880
- Labeler code
- 60505
- Product ID
- 60505-2880_89c200d6-4689-189a-1912-65e309c306e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA200172
- Marketing category
- ANDA
- Marketing start
- 2013-07-15
- Marketing end
- 2021-09-30
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| RANITIDINE HYDROCHLORIDE | ACTIVE INGREDIENT | BK76465IHM | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| RANITIDINE | ACTIVE MOIETY | 884KT10YB7 | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| CARNAUBA WAX | INACTIVE INGREDIENT | R12CBM0EIZ | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| POLYDEXTROSE | INACTIVE INGREDIENT | VH2XOU12IE | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| VANILLIN | INACTIVE INGREDIENT | CHI530446X | RANITIDINE (RANITIDINE HYDROCHLORIDE) TABLET, FILM COATED [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-2880-7 | 60505288007 | 10000 TABLET, FILM COATED in 1 BOTTLE (60505-2880-7) | 2013-07-15 | 2021-09-30 | No | No | Current |