Ranitidine
- Product NDC
- 37808-302
- 11-digit product format
- 378080302
- Labeler code
- 37808
- Product ID
- 37808-302_8c625e29-0b7c-f00a-0fc6-7709c52c10a2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H-E-B
- Application
- ANDA200172
- Marketing category
- ANDA
- Marketing start
- 2018-01-24
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-302-01 | 37808030201 | 1 BOTTLE in 1 CARTON (37808-302-01) > 130 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-01-24 | 0000-00-00 | No | No | Current |
| 37808-302-02 | 37808030202 | 1 BOTTLE in 1 CARTON (37808-302-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-01-24 | 0000-00-00 | No | No | Current |
| 37808-302-06 | 37808030206 | 1 BOTTLE in 1 CARTON (37808-302-06) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2018-01-24 | 0000-00-00 | No | No | Current |